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Article

Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia.

Journal of human genetics - 1 Nov 2010

Dzhemileva Lilya U, Barashkov Nikolay A, Posukh Olga L, Khusainova Rita I, Akhmetova Vita L, Kutuev Ildus A, Gilyazova Irina R, Tadinova Vera N, Fedorova Sardana A, Khidiyatova Irina M, Lobov Simeon L, Khusnutdinova Elza K

Abstract excerpt

Hearing impairment is one of the most common disorders of sensorineural function and the incidence of profound prelingual deafness is about 1 per 1000 at birth. GJB2 gene mutations make the largest contribution to hereditary hearing impairment. The spectrum and prevalence of some GJB2 mutations a...

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Identifiers

PMID: 20739944
DOI: 10.1038/jhg.2010.101

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20739944-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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