The association between GJB2 mutation and GJB6 gene in non syndromic hearing loss school children
Recently, molecular testing for GJB2 mutations has become the standard of care for the diagnosis of patients with non syndromic hearing impairment of unknown cause. The aims of this study are to determine the association between GJB2 mutation and GJB6 and to report the variation of mutations in deaf...
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| Format: | Journal |
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Medical Journal of Malaysia, Malaysian Medical Association
2011
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| Online Access: | http://www.myjurnal.my/public/article-view.php?id=12585 |