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Article

Spectrum of GJB2 mutations in a cohort of nonsyndromic hearing loss cases from the Kingdom of Saudi Arabia.

Genetic testing and molecular biomarkers - 1 Feb 2010

Al-Qahtani Mohammed H, Baghlab Ibtessam, Chaudhary Adeel G, Abuzenadah Adel M, Bamanie Afaf, Daghistani Kamal J, Safieh Malek, Fida Loai, Dallol Ashraf

Abstract excerpt

Nonsyndromic hearing loss (NSHL) affects a substantial proportion of newborns in the world every year. This proportion increases proportionally with the degree of consanguineous marriages in any society. In the Kingdom of Saudi Arabia, consanguineous marriages are common practice and this is associated with a noticeably high frequency of inherited conditions affecting the resulting progeny, including NSHL. Until...

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Identifiers

PMID: 19929407
DOI: 10.1089/gtmb.2009.0111

Genes

GJB2

Provenance

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