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A systematic review and meta-analysis of 235delC mutation of <it>GJB2</it> gene

<p>Abstract</p> <p>Background</p> <p>The 235delC mutation of <it>GJB2</it> 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.</p> <p>Methods</p> <p>A sy...

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Bibliografische gegevens
Hoofdauteurs: Yao Jun, Lu Yajie, Wei Qinjun, Cao Xin, Xing Guangqian
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMC 2012-07-01
Reeks:Journal of Translational Medicine
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Online toegang:http://www.translational-medicine.com/content/10/1/136
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