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Mitochondrial deafness mutations reviewed
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Mitochondrial deafness mutations reviewed
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
main subject
mitochondrial deafness
1 reference
based on heuristic
inferred from title
deafness
1 reference
based on heuristic
inferred from title
author name string
Fischel-Ghodsian N
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
publication date
1 January 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
published in
Human Mutation
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
volume
13
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
page(s)
261-270
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
cites work
Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Biogenesis of mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12s rRNA gene: evidence of heteroplasmy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mitochondrial genetics and hearing loss: the missing link between genotype and phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mitochondrial mutation associated with nonsyndromic deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Decoding at the ribosomal A site: antibiotics, misreading and energy of aminoacyl-tRNA binding.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Genetic aspects of antibiotic induced deafness: mitochondrial inheritance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
A molecular basis for human hypersensitivity to aminoglycoside antibiotics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Sensorineural deafness inherited as a tissue specific mitochondrial disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Presence of mitochondrial large ribosomal RNA outside mitochondria in germ plasm of Drosophila melanogaster.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
FAMILIAL SENSITIVITY TO STREPTOMYCIN.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mitochondrial DNA mutations and pathogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Screening for mtDNA diabetes mutations in Pima Indians with NIDDM.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Cochlear origin of hearing loss in MELAS syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case report.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Diseases of the mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
H-2M3 encodes the MHC Class I molecule presenting the maternally transmitted antigen of the mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C261%3A%3AAID-HUMU1%3E3.0.CO%3B2-W
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
PubMed ID
10220138
1 reference
stated in
Europe PubMed Central
PubMed ID
10220138
retrieved
28 July 2017
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