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Meta-Analysis of GJB2 Mutation 35delG Frequencies in Europe

✍ Scribed by Lucotte, Gerard; Mercier, Geraldine


Book ID
120927681
Publisher
Mary Ann Liebert
Year
2001
Tongue
English
Weight
118 KB
Volume
5
Category
Article
ISSN
1090-6576

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## Abstract Mutations in __GJB2__ are a major cause of autosomal recessive non‐syndromic hearing loss (ARNSHL) in many populations. A single mutation of this gene (35delG) accounts for approximately 70% of __GJB2__ mutations that are associated with ARNSHL in Caucasians in many European countries a