Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
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DOI: 10.1089/gtmb.2016.0328
Abstract: AIM To investigate the causative genetic mutations in 12 Pakistani families with nonsyndromic or syndromic hearing loss. METHODS Mutations in the most common causative gene for hearing loss, GJB2, were evaluated by Sanger sequencing. Targeted… read more here.
Keywords: hearing loss; loss; nonsyndromic syndromic; families nonsyndromic ... See more keywords