Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia

The mutations in theGJB2(Сх26) gene make the biggest contribution to hereditary hearing loss. The spectrum and prevalence of theGJB2gene mutations are specific to populations of different ethnic origins. For severalGJB2 mutations, their origin from appropriate ancestral founder chromosome was shown,...

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Detalhes bibliográficos
Main Authors: Dzhemileva, L.U., Posukh, O.L., Barashkov, N.A., Fedorova, S.A., Teryutin, F.M., Akhmetova, 
V.L., Khidiyatova, I.M., Khusainova, R.I., Lobov, S.L., Khusnutdinova, E.K.
Formato: Artigo
Idioma:Inglês
Publicado em: A.I. Gordeyev 2011
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3347605/
https://ncbi.nlm.nih.gov/pubmed/22649694
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