Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

• Główni autorzy: Marina V. Zytsar (Autor), Nikolay A. Barashkov (Autor), Marita S. Bady-Khoo (Autor), Olga A. Shubina-Olejnik (Autor), Nina G. Danilenko (Autor), Alexander A. Bondar (Autor), Igor V. Morozov (Autor), Aisen V. Solovyev (Autor), Valeriia Yu. Danilchenko (Autor), Vladimir N. Maximov (Autor), Olga L. Posukh (Autor)
• Format: Książka
• Wydane: BMC, 2018-08-01T00:00:00Z.
• Hasła przedmiotowe: article
• Dostęp online: Connect to this object online.

Abstract Background Mutations in GJB2 gene are a major causes of deafness and their spectrum and prevalence are specific for various populations. The well-known mutation c.35delG is more frequent in populations of Caucasian origin. Data on the c.35delG prevalence in Russia are mainly restricted to t...