Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method-Reference-Cited by-同舟云学术

Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method

Published:1999 Issue:3 Volume:14 Page:263-266
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Storm Katrien,Willocx Sandra,Flothmann Kris,Van Camp Guy

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference13 articles.

1. Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations

2. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

3. Connexin-26 mutations in sporadic and inherited sensorineural deafness

4. Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss

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4. Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia;BMC Medical Genetics;2018-08-07

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