Article
A systematic review and meta-analysis of 235delC mutation of GJB2 gene.
Journal of translational medicine - 2 Jul 2012
Yao Jun, Lu Yajie, Wei Qinjun, Cao Xin, Xing Guangqian
Abstract excerpt
BACKGROUND: The 235delC mutation of GJB2 gene is considered as a risk factor for the non-syndromic hearing loss (NSHL), and a significant difference in the frequency and distribution of the 235delC mutation has been described world widely. METHODS: A systematic review was performed by means of a meta-analysis to evaluate the influence of the 235delC mutation on the risk of NSHL. A literature search in electronic...
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