Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss.
about
Modifiers of hearing impairment in humans and mice.Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency.[Etiologic profile of severe and profound sensorineural hearing loss in children in the region of north-central Morocco].In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genesMutations in CLDN14 are associated with different hearing thresholds.Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2.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 ChineseDigenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype.Connexin gene mutations among Ugandan patients with nonsyndromic sensorineural hearing loss.Molecular cloning and evolutionary analysis of the GJA1 (connexin43) gene from bats (Chiroptera).Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.Connexin 26 and 30 mutations in paediatric patients with congenital, non-syndromic hearing loss treated with cochlear implantation in Mediterranean Turkey.Connexin 43 and hearing: possible implications for retrocochlear auditory processing.Research of genetic bases of hereditary non-syndromic hearing loss.DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes.Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family.Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects.Lower carrier rate of GJB2 W24X ancestral Indian mutation in Roma samples from Hungary: implication for public health intervention.Double heterozygosity with mutations involving both the GJB2 and GJB6 genes is a possible, but very rare, cause of congenital deafness in the Czech population.Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss.
P2860
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P2860
Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@ast
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@en
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@nl
type
label
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@ast
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@en
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@nl
prefLabel
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@ast
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@en
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@nl
P2093
P1433
P1476
Frequencies of gap- and tight- ...... ve non-syndromic hearing loss.
@en
P2093
A Ghanbari
M Emiroglu
M Yuksel-Apak
P356
10.1034/J.1399-0004.2003.00101.X
P577
2003-07-01T00:00:00Z