A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13
about
Nonsyndromic hearing impairment: unparalleled heterogeneityA gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneCochlin produced by follicular dendritic cells promotes antibacterial innate immunityInnate immune recognition of molds and homology to the inner ear protein, cochlin, in patients with autoimmune inner ear diseaseA gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.Molecular markers for cell types of the inner ear and candidate genes for hearing disordersBeginning of a molecular era in hearing and deafness.Linkage analysis in Usher syndrome type I (USH1) families from SpainNon-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from PakistanHuman sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss loci.Extralabyrinthine manifestations of DFNA9Non-syndromic autosomal-dominant deafness.The genetics of Ménière's disease.Genetic disorders of the vestibular system.Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA bindingCochlin isoforms and their interaction with CTL2 (SLC44A2) in the inner ear.Murine autoimmune hearing loss mediated by CD4+ T cells specific for inner ear peptides.Genes responsible for human hereditary deafness: symphony of a thousand.c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.Reply to niermeijer.Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH.Does Otovestibular Loss in the Autosomal Dominant Disorder DFNA9 Have an Impact of on Cognition? A Systematic Review.Phenotype description of a novel DFNA9/COCH mutation, I109T.Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family.A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13."New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family.The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
P2860
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P2860
A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13
description
1996 nî lūn-bûn
@nan
1996 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@ast
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@en
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@nl
type
label
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@ast
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@en
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@nl
prefLabel
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@ast
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@en
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@nl
P2093
P356
P1476
A gene for non-syndromic autos ...... ss maps to chromosome 14q12-13
@en
P2093
C E Seidman
E N Manolis
J G Seidman
P304
P356
10.1093/HMG/5.7.1047
P407
P577
1996-07-01T00:00:00Z