(Q37258743)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

review article

1 reference

title

Molecular pathology of myofibrillar myopathies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

1

Isidre Ferrer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

publication date

3 September 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

Expert Reviews in Molecular Medicine

13 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

page(s)

e25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

The role of the ubiquitin-proteasome pathway in MHC class I antigen processing: implications for vaccine design.

13 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

For whom the bell tolls: protein quality control of the endoplasmic reticulum and the ubiquitin-proteasome connection

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Genome-wide analysis of repressor element 1 silencing transcription factor/neuron-restrictive silencing factor (REST/NRSF) target genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The neuron-restrictive silencer factor (NRSF): a coordinate repressor of multiple neuron-specific genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Target genes of neuron-restrictive silencer factor are abnormally up-regulated in human myotilinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Myotilin overexpression enhances myopathology in the LGMD1A mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Transgenic mice expressing the myotilin T57I mutation unite the pathology associated with LGMD1A and MFM

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The biology of desmin filaments: how do mutations affect their structure, assembly, and organisation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Truncated desmin in PtK2 cells induces desmin-vimentin-cytokeratin coprecipitation, involution of intermediate filament networks, and nuclear fragmentation: a model for many degenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Mouse model of desmin-related cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Syncoilin accumulation in two patients with desmin-related myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Zaspopathy in a large classic late-onset distal myopathy family

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Different early pathogenesis in myotilinopathy compared to primary desminopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

A mutation in myotilin causes spheroid body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

myotilin Mutation found in second pedigree with LGMD1A

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Myotilin is mutated in limb girdle muscular dystrophy 1A

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Alpha B-crystallin mutation in dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

A novel desmin R355P mutation causes cardiac and skeletal myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segment

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Desmin splice variants causing cardiac and skeletal myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Desmin mutation responsible for idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Loss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Indications for a novel muscular dystrophy pathway. gamma-filamin, the muscle-specific filamin isoform, interacts with myotilin

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Molecular cloning of human ABPL, an actin-binding protein homologue

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Filamins as integrators of cell mechanics and signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Myozenin: an alpha-actinin- and gamma-filamin-binding protein of skeletal muscle Z lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Structural and functional aspects of filamins

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The limits of promiscuity: isoform-specific dimerization of filamins

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Zasp is required for the assembly of functional integrin adhesion sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Zebrafish cypher is important for somite formation and heart development

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Characterization and in vivo functional analysis of splice variants of cypher

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Solution structure of ZASP PDZ domain; implications for sarcomere ultrastructure and enigma family redundancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

ZASP: a new Z-band alternatively spliced PDZ-motif protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Targeted Deletion of the Muscular Dystrophy Gene myotilin Does Not Perturb Muscle Structure or Function in Mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Actin-organising properties of the muscular dystrophy protein myotilin

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Myotilin, the limb-girdle muscular dystrophy 1A (LGMD1A) protein, cross-links actin filaments and controls sarcomere assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The function of alpha-crystallin in vision

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Human alpha B-crystallin (CRYA2) gene mapped to chromosome 11q12-q23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Null mutation in the desmin gene gives rise to a cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Disruption of muscle architecture and myocardial degeneration in mice lacking desmin

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Cardiovascular lesions and skeletal myopathy in mice lacking desmin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Conserved segments 1A and 2B of the intermediate filament dimer: their atomic structures and role in filament assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The intermediate filament protein consensus motif of helix 2B: its atomic structure and contribution to assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Intermediate filaments: structural conservation and divergence

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Human desmin-coding gene: complete nucleotide sequence, characterization and regulation of expression during myogenesis and development

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Intermediate filaments: molecular structure, assembly mechanism, and integration into functionally distinct intracellular Scaffolds

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Pathological consequences of VCP mutations on human striated muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Myotilinopathy: refining the clinical and myopathological phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Myofibrillar myopathy caused by novel dominant negative alpha B-crystallin mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Familial conformational diseases and dementias

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Medicine: danger--misfolding proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Cellular defenses against unfolded proteins: a cell biologist thinks about neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

21 January 2018

Conformational disease

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Surplus protein myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Gene-related protein surplus myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Mutations in ZASP define a novel form of muscular dystrophy in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Mutations in myotilin cause myofibrillar myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The sarcomeric Z-disc: a nodal point in signalling and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

A dysfunctional desmin mutation in a patient with severe generalized myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Mitochondrial dysfunction in myofibrillar myopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Degradation of oxidized proteins by the 20S proteasome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Proteasome mediates removal of proteins oxidized during myocardial ischemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Proteasomal defense of oxidative protein modifications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Sarcolemmal damage in dystrophin deficiency is modulated by synergistic interactions between mechanical and oxidative/nitrosative stresses

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Patients with dystrophinopathy show evidence of increased oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The RAGE pathway in inflammatory myopathies and limb girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Mitochondrial disease in mouse results in increased oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Oxidative stress and the pathogenesis of muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Gender-specific proteomic alterations in glycolytic and mitochondrial pathways in aging monkey hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Identification of specific oxidatively modified proteins in chicken muscles using a combined immunologic and proteomic approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The kinase domain of titin controls muscle gene expression and protein turnover

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Morphogenesis of Lewy bodies: dissimilar incorporation of alpha-synuclein, ubiquitin, and p62.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

p62 Is a common component of cytoplasmic inclusions in protein aggregation diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Sequestosome 1/p62 is a polyubiquitin chain binding protein involved in ubiquitin proteasome degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Sequestosome 1/p62--more than just a scaffold

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Aggresome formation in liver cells in response to different toxic mechanisms: role of the ubiquitin-proteasome pathway and the frameshift mutant of ubiquitin

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Frameshift mutants of beta amyloid precursor protein and ubiquitin-B in Alzheimer's and Down patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Distinct chaperone mechanisms can delay the formation of aggresomes by the myopathy-causing R120G alphaB-crystallin mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Lewy-body formation is an aggresome-related process: a hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Conformational diseases: an umbrella for various neurological disorders with an impaired ubiquitin-proteasome system

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Desmin - Protein Surplus Myopathies, 96th European Neuromuscular Centre (ENMC)-sponsored International Workshop held 14-16 September 2001, Naarden, The Netherlands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Desmin-related neuromuscular disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

The Mallory body as an aggresome: in vitro studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Aggresomes, inclusion bodies and protein aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Clusterin solubility and aggregation in Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Nitric oxide synthase in muscular dystrophies: a re-evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Intermediate filaments as mechanical integrators of cellular space

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

Expression of R120G-alphaB-crystallin causes aberrant desmin and alphaB-crystallin aggregation and cardiomyopathy in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Oxidative Stress in Desminopathies and Myotilinopathies: A Link between Oxidative Damage and Abnormal Protein Aggregation

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and electron microscopy analysis of 10 cases

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Myofibrillar myopathy. III. Abnormal expression of cyclin-dependent kinases and nuclear proteins

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathy

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Impact of disease mutations on the desmin filament assembly process

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Protein aggregate myopathies

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Binding of the stress protein alpha B-crystallin to cardiac myofibrils correlates with the degree of myocardial damage during ischemia/reperfusion in vivo

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Characterization of muscle filamin isoforms suggests a possible role of gamma-filamin/ABP-L in sarcomeric Z-disc formation

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathies

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria.

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Involvement of clusterin and the aggresome in abnormal protein deposits in myofibrillar myopathies and inclusion body myositis.

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

Desmin Is Oxidized and Nitrated in Affected Muscles in Myotilinopathies and Desminopathies

1 reference

https://api.crossref.org/works/10.1017%2FS1462399408000793

7 January 2021

10.1017/S1462399408000793

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18764962%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

1 reference