High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss-Reference-Cited by-同舟云学术

High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss

Published:2005 Issue:3 Volume:137A Page:255-258
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Álvarez Araceli,del Castillo Ignacio,Villamar Manuela,Aguirre Luis A.,González-Neira Anna,López-Nevot Alicia,Moreno-Pelayo Miguel A.,Moreno Felipe

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference39 articles.

1. Prevalent connexin 26 gene (GJB2) mutations in Japanese

2. Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients

3. Connexin 26 R143W Mutation Associated with Recessive Nonsyndromic Sensorineural Deafness in Africa

4. Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

5. A comprehensive genetic map of the human genome based on 5,264 microsatellites

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