A large cohort study ofGJB2mutations in Japanese hearing loss patients
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01407.x/fullpdf
Reference26 articles.
1. Prevalent connexin 26 gene (GJB2) mutations in Japanese;Abe;J Med Genet,2000
2. GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation;Ohtsuka;Hum Genet,2003
3. Connexin26 mutations associated with nonsyndromic hearing loss;Park;Laryngoscope,2000
4. The prevalence of connexin 26 ( GJB2) mutations in the Chinese population;Liu;Hum Genet,2002
5. Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan;Wang;Eur J Hum Genet,2002
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