Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
about
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 Cx31Mutation analysis of the Cx26, Cx30, and Cx31 genes in autosomal recessive nonsyndromic hearing impairment.Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss.Functional interaction between mesenchymal stem cells and spiral ligament fibrocytes.A new mutation in the GJB3 gene in a patient with erythrokeratodermia variabilis.
P2860
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
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2003 nî lūn-bûn
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2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած
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2003 թվականի փետրվարին հրատարակված գիտական հոդված
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2003年の論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年论文
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name
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@ast
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@en
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@nl
type
label
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@ast
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@en
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@nl
prefLabel
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@ast
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@en
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@nl
P2093
P1433
P1476
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
@en
P2093
P356
10.1034/J.1399-0004.2003.00031.X
P407
P577
2003-02-01T00:00:00Z