about
Age-related hearing impairment and the triad of acquired hearing loss.The bacterial and mitochondrial ribosomal A-site molecular switches possess different conformational substatesGJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE reviewA study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China.Mitochondrial DNA (mtDNA) haplotypes and dysfunctions in presbyacusisFamilial aggregation of age-related hearing loss in an epidemiological study of older adults.Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.Noise-induced hearing loss in mice treated with antiretroviral drugs.Analysis of mitochondrial DNA sequences in childhood encephalomyopathies reveals new disease-associated variantsCommon molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment.Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genome.The genetic bases for non-syndromic hearing loss among ChineseHereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis.Mitochondrial rRNA and tRNA and hearing function.Audiologic and genetic features of the A3243G mtDNA mutationNew clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS)Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects.Genetics of hearing loss: where are we standing now?Cochlear epithelial of dog fetuses: a new source of multipotent stem cells.Audiological and genetic features of the mtDNA mutations.Hearing loss in mitochondrial disorders.Audiological and radiological characteristics of a family with T961G mitochondrial mutation.Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss.Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy.The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.Perda auditiva genética
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
name
Mitochondrial defects and hearing loss.
@ast
Mitochondrial defects and hearing loss.
@en
Mitochondrial defects and hearing loss.
@nl
type
label
Mitochondrial defects and hearing loss.
@ast
Mitochondrial defects and hearing loss.
@en
Mitochondrial defects and hearing loss.
@nl
prefLabel
Mitochondrial defects and hearing loss.
@ast
Mitochondrial defects and hearing loss.
@en
Mitochondrial defects and hearing loss.
@nl
P356
P1476
Mitochondrial defects and hearing loss.
@en
P2093
Cortopassi GA
Hutchin TP
P2888
P304
P356
10.1007/PL00000673
P577
2000-12-01T00:00:00Z