The35delGMutation in the Connexin 26 Gene (GJB2) Associated with Congenital Deafness: European Carrier Frequencies and Evidence for Its Origin in Ancient Greece-Reference-Cited by-同舟云学术

The35delGMutation in the Connexin 26 Gene (GJB2) Associated with Congenital Deafness: European Carrier Frequencies and Evidence for Its Origin in Ancient Greece

Published:2005-03 Issue:1 Volume:9 Page:20-25
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Lucotte Gérard¹,Diéterlen Florent¹

Affiliation:

1. Institute of Molecular Anthropology, 75005 Paris, France.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/gte.2005.9.20

Reference36 articles.

1. Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation

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

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

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