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,...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: A.I. Gordeyev 2011
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3347605/
https://ncbi.nlm.nih.gov/pubmed/22649694
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia