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

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 the Europ...

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Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: Zytsar, Marina V., Barashkov, Nikolay A., Bady-Khoo, Marita S., Shubina-Olejnik, Olga A., Danilenko, Nina G., Bondar, Alexander A., Morozov, Igor V., Solovyev, Aisen V., Danilchenko, Valeriia Yu., Maximov, Vladimir N., Posukh, Olga L.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2018
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6081885/
https://ncbi.nlm.nih.gov/pubmed/30086704
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0650-5
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