Literature DB >> 12068628

[Frequency of the 35delG mutation of the connexin 26 gene (GJB2) in patients with non-syndromic autosome-recessive deafness from Bashkortostan and in ethnic groups of the Volga-Ural region].

I M Khidiiatova1, L U Dzhemileva, R M Khabibulin, E K Khusnutdinova.   

Abstract

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Year:  2002        PMID： 12068628

Source DB:  PubMed          Journal:  Mol Biol (Mosk)        ISSN： 0026-8984


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  4 in total

1.  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.

Authors:  L U Dzhemileva; O L Posukh; N A Barashkov; S A Fedorova; F M Teryutin; V L Akhmetova; I M Khidiyatova; R I Khusainova; S L Lobov; E K Khusnutdinova
Journal:  Acta Naturae       Date:  2011-07       Impact factor: 1.845

2.  Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families.

Authors:  Jeong-In Baek; Se-Kyung Oh; Dong-Bin Kim; Soo-Young Choi; Un-Kyung Kim; Kyu-Yup Lee; Sang-Heun Lee
Journal:  Orphanet J Rare Dis       Date:  2012-09-03       Impact factor: 4.123

3.  First molecular screening of deafness in the Altai Republic population.

Authors:  Olga Posukh; Nathalie Pallares-Ruiz; Vera Tadinova; Ludmila Osipova; Mireille Claustres; Anne-Françoise Roux
Journal:  BMC Med Genet       Date:  2005-03-24       Impact factor: 2.103

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

Authors:  Marina V Zytsar; Nikolay A Barashkov; Marita S Bady-Khoo; Olga A Shubina-Olejnik; Nina G Danilenko; Alexander A Bondar; Igor V Morozov; Aisen V Solovyev; Valeriia Yu Danilchenko; Vladimir N Maximov; Olga L Posukh
Journal:  BMC Med Genet       Date:  2018-08-07       Impact factor: 2.103
  4 in total

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