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Changes in the connexin 26 gene (GJB2) in Russian patients with hearing loss: Results of long-term molecular diagnostics of hereditary nonsyndromic hearing loss

✍ Scribed by E. A. Bliznetz; V. A. Galkina; G. N. Matyushchenko; A. G. Kisina; T. G. Markova; A. V. Polyakov


Book ID
114990885
Publisher
SP MAIK Nauka/Interperiodica
Year
2012
Tongue
English
Weight
490 KB
Volume
48
Category
Article
ISSN
1022-7954

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Hereditary hearing loss (HHL) is one of the most common congenital disorders and is highly heterogeneous. Mutations in the connexin 26 (CX26) gene (GJB2) account for about 20% of all cases of childhood deafness, and approach 50% in documented recessive cases of non-syndromic hearing loss. In additio