Spectrum of Genetic Changes in Patients with Non-Syndromic Hearing Impairment and Extremely High Carrier Frequency of 35delG GJB2 Mutation in Belarus

The genetic nature of sensorineural hearing loss (SNHL) has so far been studied for many ethnic groups in various parts of the world. The single-nucleotide guanine deletion (35delG) of the GJB2 gene coding for connexin 26 was shown to be the main genetic cause of autosomal recessive deafness among E...

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Detalles Bibliográficos
Autores principales: Danilenko, Nina, Merkulava, Elena, Siniauskaya, Marina, Olejnik, Olga, Levaya-Smaliak, Anastasia, Kushniarevich, Alena, Shymkevich, Andrey, Davydenko, Oleg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342211/
https://www.ncbi.nlm.nih.gov/pubmed/22567152
http://dx.doi.org/10.1371/journal.pone.0036354

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342211/
https://www.ncbi.nlm.nih.gov/pubmed/22567152
http://dx.doi.org/10.1371/journal.pone.0036354

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