(Q33346003)

26 July 2017

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title

Human hereditary hearing impairment: mouse models can help to solve the puzzle (English)

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26 July 2017

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Guy Van Camp

3

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author name string

Karen Vrijens

series ordinal

1

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26 July 2017

Lut Van Laer

series ordinal

2

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26 July 2017

publication date

11 September 2008

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26 July 2017

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26 July 2017

volume

124

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26 July 2017

issue

4

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26 July 2017

page(s)

325-348

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A fast motile response in guinea-pig outer hair cells: the cellular basis of the cochlear amplifier

26 July 2017

cites work

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https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

Genetic associations in age-related hearing thresholds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

Ca2+ signaling in the inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

Mitochondrial DNA deletions associated with aging and presbyacusis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

21 January 2018

1 reference

12 December 2020

The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system

1 reference

12 December 2020

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

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12 December 2020

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

1 reference

12 December 2020

Cross-links between stereocilia in the guinea pig cochlea.

1 reference

12 December 2020

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

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12 December 2020

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

1 reference

12 December 2020

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

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12 December 2020

Unconventional myosins in cell movement, membrane traffic, and signal transduction

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12 December 2020

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

1 reference

12 December 2020

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

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12 December 2020

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

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12 December 2020

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

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12 December 2020

A multivalent PDZ-domain protein assembles signalling complexes in a G-protein-coupled cascade

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12 December 2020

Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.

1 reference

12 December 2020

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

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12 December 2020

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12 December 2020

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

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12 December 2020

Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.

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12 December 2020

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

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12 December 2020

Gap junction systems in the mammalian cochlea

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12 December 2020

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

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12 December 2020

The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15

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12 December 2020

Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2

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12 December 2020

Morphological differences among radial afferent fibers in the cat cochlea: an electron-microscopic study of serial sections

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12 December 2020

Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia

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12 December 2020

DNA damage by oxygen-derived species Its mechanism and measurement in mammalian systems

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12 December 2020

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

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12 December 2020

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

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12 December 2020

Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus

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12 December 2020

Classical cadherin adhesion molecules: coordinating cell adhesion, signaling and the cytoskeleton

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12 December 2020

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

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12 December 2020

Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss

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12 December 2020

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss

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12 December 2020

Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice

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12 December 2020

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

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12 December 2020

Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.

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12 December 2020

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

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12 December 2020

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

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12 December 2020

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

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12 December 2020

Defective myosin VIIA gene responsible for Usher syndrome type 1B

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12 December 2020

Gender differences in a longitudinal study of age-associated hearing loss.

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12 December 2020

Genetic and environmental influences on self-reported reduced hearing in the old and oldest old.

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12 December 2020

Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene

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12 December 2020

Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.

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12 December 2020

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

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12 December 2020

Unconventional myosins in inner-ear sensory epithelia

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12 December 2020

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

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12 December 2020

Developmental expression patterns of connexin26 and -30 in the rat cochlea

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12 December 2020

In vitro and in vivo suppression of GJB2 expression by RNA interference.

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12 December 2020

Development of the hair bundle and mechanotransduction

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12 December 2020

Anatomy of cochlear innervation

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12 December 2020

Association of mitochondrial DNA deletions and cochlear pathology: a molecular biologic tool

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12 December 2020

Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.

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12 December 2020

Electrokinetic shape changes of cochlear outer hair cells

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12 December 2020

A mechanism for active hearing

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12 December 2020

Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study

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12 December 2020

A new age in the genetics of deafness

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12 December 2020

Novel frameshift mutations in the procollagen 2 gene (COL2A1) associated with Stickler syndrome (hereditary arthro-ophthalmopathy)

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12 December 2020

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

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12 December 2020

Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population.

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12 December 2020

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

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12 December 2020

Evoked mechanical responses of isolated cochlear outer hair cells

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12 December 2020

Elongation of hair cell stereocilia is defective in the mouse mutant whirler

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12 December 2020

Vlgr1 knockout mice show audiogenic seizure susceptibility.

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12 December 2020

Knockout mouse models in pain research

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12 December 2020

Mapping quantitative trait loci for hearing loss in Black Swiss mice

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12 December 2020

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment.

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12 December 2020

Histopathology and molecular genetics of hearing loss in the human

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12 December 2020

Transgenic and gene knock-out techniques and burn research.

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12 December 2020

Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).

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12 December 2020

Regulation of electromotility in the cochlear outer hair cell

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12 December 2020

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

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12 December 2020

Claudin-based barrier in simple and stratified cellular sheets

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12 December 2020

A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9

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12 December 2020

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

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12 December 2020

A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice.

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12 December 2020

Identification and characterisation of human Junctional Adhesion Molecule (JAM)

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12 December 2020

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

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12 December 2020

Genotype-phenotype correlations for SLC26A4-related deafness.

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12 December 2020

Correlation of Cochlear Blood Supply with Mitochondrial DNA Common Deletion in Presbyacusis

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12 December 2020

Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)

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12 December 2020

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.

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12 December 2020

A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

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12 December 2020

Description and primary results from an audiometric study of male twins

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12 December 2020

GATA3 haplo-insufficiency causes human HDR syndrome

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12 December 2020

Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss

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12 December 2020

Two quantitative trait loci affecting progressive hearing loss in 101/H mice.

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12 December 2020

Rapid renewal of auditory hair bundles

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12 December 2020

Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse

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12 December 2020

Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice

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12 December 2020

Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice

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12 December 2020

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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12 December 2020

PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse

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12 December 2020

Multifunctional strands in tight junctions

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12 December 2020

The role of outer hair cell motility in cochlear tuning

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12 December 2020

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

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12 December 2020

Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle

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12 December 2020

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration

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12 December 2020

Gap junctions and cochlear homeostasis

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12 December 2020

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

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12 December 2020

Espins are multifunctional actin cytoskeletal regulatory proteins in the microvilli of chemosensory and mechanosensory cells

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12 December 2020

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

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12 December 2020

Ahl3, a third locus on mouse chromosome 17 affecting age-related hearing loss.

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12 December 2020

From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

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12 December 2020

A deafness mutation isolates a second role for the tectorial membrane in hearing

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12 December 2020

Cochlear dysfunction in the jerker mouse

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12 December 2020

Noise-induced transient microlesions in the cell membranes of auditory hair cells.

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12 December 2020

Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development

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12 December 2020

Identification of mutations in members of the connexin gene family as a cause of nonsyndromic deafness in Taiwan.

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12 December 2020

Auditory function associated with Col11a1 haploinsufficiency in chondrodysplasia (cho) mice.

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12 December 2020

The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions

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12 December 2020

Role of myosin VI in the differentiation of cochlear hair cells

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12 December 2020

The fine structure of freeze-fractured intercellular junctions in the guinea pig inner ear

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12 December 2020

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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12 December 2020

K+ cycling and the endocochlear potential

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12 December 2020

Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness

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12 December 2020

Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

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12 December 2020

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

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12 December 2020

Connexin 26 as a cause of hereditary hearing loss.

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12 December 2020

NMR structure of the LCCL domain and implications for DFNA9 deafness disorder

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12 December 2020

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

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12 December 2020

Isolation of a gene encoding a novel member of the nuclear receptor superfamily from the critical region of Usher syndrome type IIa at 1q41

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12 December 2020

Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification

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12 December 2020

Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease

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12 December 2020

A mutation in PDS causes non-syndromic recessive deafness

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12 December 2020

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

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12 December 2020

Chemical dissection of stereovilli from fish inner ear reveals differences from intestinal microvilli

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12 December 2020

Development and properties of stereociliary link types in hair cells of the mouse cochlea

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12 December 2020

Stickler syndrome. A mutation in the nonhelical 3' end of type II procollagen gene

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12 December 2020

Ultrastructural findings in the inner ear of Jackson shaker mice

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12 December 2020

Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II

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12 December 2020

Nuclear and mitochondrial genes mutated in nonsyndromic impaired hearing

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12 December 2020

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.

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12 December 2020

The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.

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12 December 2020

Cadherin 23 is a component of the tip link in hair-cell stereocilia

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12 December 2020

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

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12 December 2020

An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal

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12 December 2020

The 3D structure of the tectorial membrane determined by second-harmonic imaging microscopy

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12 December 2020

Interactions in the network of Usher syndrome type 1 proteins

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12 December 2020

The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency

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12 December 2020

Blindness and auditory impairment caused by loss of the sodium bicarbonate cotransporter NBC3

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12 December 2020

Initial sequencing and comparative analysis of the mouse genome

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12 December 2020

Plasma membrane Ca2+-ATPase extrudes Ca2+ from hair cell stereocilia

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12 December 2020

Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness

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12 December 2020

mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)

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12 December 2020

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

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12 December 2020

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

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12 December 2020

Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells

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12 December 2020

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

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12 December 2020

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

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12 December 2020

The need for universal neonatal hearing screening--some aspects of epidemiology and identification

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12 December 2020

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

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12 December 2020

Cross-links between stereocilia in the guinea pig organ of Corti, and their possible relation to sensory transduction

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12 December 2020

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

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12 December 2020

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

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12 December 2020

A type VII myosin encoded by the mouse deafness gene shaker-1

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12 December 2020

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

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12 December 2020

Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia

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12 December 2020

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

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12 December 2020

The Origin of Jerker, a New Gene Mutation of the House Mouse, and Linkage Studies Made with It

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12 December 2020

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss

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12 December 2020

Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

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12 December 2020

Expression pattern and functional characterization of connexin29 in transgenic mice.

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12 December 2020

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

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12 December 2020

Composition and supramolecular organization of the tectorial membrane.

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12 December 2020

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

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12 December 2020

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

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12 December 2020

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

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12 December 2020

The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.

1 reference

12 December 2020

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

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12 December 2020

Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse

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12 December 2020

Molecular mechanisms of age-related hearing loss

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12 December 2020

Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4)

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12 December 2020

DFNA9 is a progressive audiovestibular dysfunction with a microfibrillar deposit in the inner ear.

1 reference

12 December 2020

Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells

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12 December 2020

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

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12 December 2020

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

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12 December 2020

Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death

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12 December 2020

Mutations of human TMHS cause recessively inherited non-syndromic hearing loss

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12 December 2020

Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding

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12 December 2020

The circling mouse (C57BL/6J-cir) has a 40-kilobase genomic deletion that includes the transmembrane inner ear (tmie) gene

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12 December 2020

Mutations of MYO6 are associated with recessive deafness, DFNB37

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12 December 2020

Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness

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12 December 2020

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

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12 December 2020

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

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12 December 2020

The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.

1 reference

12 December 2020

Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome.

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12 December 2020

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

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12 December 2020

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

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12 December 2020

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene

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12 December 2020

Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.

1 reference

12 December 2020

Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

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12 December 2020

Acoustic startle and prepulse inhibition in 40 inbred strains of mice

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12 December 2020

Cochlear mitochondrial DNA3867bp deletion in aged mice

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12 December 2020

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1 reference

12 December 2020

Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

1 reference

12 December 2020

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous

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12 December 2020

Modification of human hearing loss by plasma-membrane calcium pump PMCA2

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12 December 2020

Cross-links between stereocilia in the human organ of Corti

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12 December 2020

Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources

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12 December 2020

Strain background effects and genetic modifiers of hearing in mice

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12 December 2020

Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells

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12 December 2020

Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus

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12 December 2020

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

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12 December 2020

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

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12 December 2020

Expression of the gap-junction connexins 26 and 30 in the rat cochlea

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12 December 2020

Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

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12 December 2020

Ahl2, a second locus affecting age-related hearing loss in mice

1 reference

12 December 2020

Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice

1 reference

12 December 2020

Eya4-deficient mice are a model for heritable otitis media

1 reference

12 December 2020

Distribution of the 275 kD hair cell antigen and cell surface specialisations on auditory and vestibular hair bundles in the chicken inner ear

1 reference

12 December 2020

Otogelin: a glycoprotein specific to the acellular membranes of the inner ear

1 reference

12 December 2020

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

1 reference

12 December 2020

Hearing: the effects of chemicals

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12 December 2020

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

1 reference

12 December 2020

A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment

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12 December 2020

10.1007/S00439-008-0556-Y

Identifiers

DOI

1 reference

Dimensions Publication ID

26 July 2017

1046264870

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1 reference