Mutation detection in GJB2 gene among Malays with non-syndromic hearing loss

Zainal SA 1 , Md Daud MK , Abd Rahman N , Zainuddin Z , Alwi Z

Affiliations 

  • 1 Human Genome Center, School of Medical Sciences, Health Campus, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia
Int J Pediatr Otorhinolaryngol, 2012 Aug;76(8):1175-9.
PMID: 22613756 DOI: 10.1016/j.ijporl.2012.04.027

Abstract

To identify the mutations in the GJB2 gene and to determine its association with non-syndromic hearing loss in Malays.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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