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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Detalles Bibliográficos
Autores principales: Yao, Jun, Lu, Yajie, Wei, Qinjun, Cao, Xin, Xing, Guangqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443034/
https://www.ncbi.nlm.nih.gov/pubmed/22747691
http://dx.doi.org/10.1186/1479-5876-10-136

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443034/
https://www.ncbi.nlm.nih.gov/pubmed/22747691
http://dx.doi.org/10.1186/1479-5876-10-136

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