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A systematic review and meta-analysis of 235delC mutation of GJB2 gene

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 met...

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Detalhes bibliográficos
Main Authors: Yao, Jun, Lu, Yajie, Wei, Qinjun, Cao, Xin, Xing, Guangqian
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3443034/
https://ncbi.nlm.nih.gov/pubmed/22747691
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-5876-10-136
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