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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Autors principals: Danilenko, Nina, Merkulava, Elena, Siniauskaya, Marina, Olejnik, Olga, Levaya-Smaliak, Anastasia, Kushniarevich, Alena, Shymkevich, Andrey, Davydenko, Oleg
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2012
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Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3342211/
https://ncbi.nlm.nih.gov/pubmed/22567152
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0036354
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