Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity
about
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing lossFrequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probandsSynergistic ototoxicity due to noise exposure and aminoglycoside antibioticsMitochondrial deafness mutations reviewed.Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing lossGenetic factors in aminoglycoside toxicity.The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness.Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.Successful MDR-TB treatment regimens including amikacin are associated with high rates of hearing loss.Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.The genetic bases for non-syndromic hearing loss among ChineseMaternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort.A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population.Mitochondrial rRNA and tRNA and hearing function.Aminoglycoside-induced vestibular injury: maintaining a sense of balance.Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: an overview study.Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.Maternally inherited nonsyndromic hearing loss.Audiological and genetic features of the mtDNA mutations.Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from MongoliaPharmGKB summary: very important pharmacogene information for MT-RNR1.Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk?Adverse effects of a single dose of gentamicin in adults: a systematic review.Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss.American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss.The search of a genetic basis for noise-induced hearing loss (NIHL).Etiologic diagnosis of sensorineural hearing loss in adults.The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.Sensorineural hearing loss and the 1555G mitochondrial DNA mutation.The Mitochondrial COI/tRNASER(UCN) G7444A Mutation may be Associated with Hearing Impairment in a Han Chinese Family.Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.
P2860
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P2860
Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity
description
1997 nî lūn-bûn
@nan
1997 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Mutation in the mitochondrial ...... eal aminoglycoside ototoxicity
@ast
Mutation in the mitochondrial ...... eal aminoglycoside ototoxicity
@en
type
label
Mutation in the mitochondrial ...... eal aminoglycoside ototoxicity
@ast
Mutation in the mitochondrial ...... eal aminoglycoside ototoxicity
@en
prefLabel
Mutation in the mitochondrial ...... eal aminoglycoside ototoxicity
@ast
Mutation in the mitochondrial ...... eal aminoglycoside ototoxicity
@en
P2093
P2860
P356
P1476
Mutation in the mitochondrial ...... eal aminoglycoside ototoxicity
@en
P2093
Batsuuri J
Dangaansuren B
Fischel-Ghodsian N
Radnaabazar J
P2860
P304
P356
10.1136/JMG.34.2.169
P407
P577
1997-02-01T00:00:00Z