Statistical study of 35delG mutation of GJB2 gene: A meta-analysis of carrier frequency
Author:
Publisher
Informa UK Limited
Subject
Speech and Hearing,Linguistics and Language,Language and Linguistics
Link
http://www.tandfonline.com/doi/pdf/10.1080/14992020802607449
Reference59 articles.
1. Prevalent connexin 26 gene (GJB2) mutations in Japanese
2. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation
3. Letter
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