Molecular characterization of autosomal recessive non syndromic hearing loss in selected families from District Mardan, Pakistan Page No: 051-056

By: Shahid Hussain, Jabar Zaman Khan Khattak, Mohammad Ismail, Qaisar Mansoor, Mohammad Haroon Khan

Keywords: Genetic hearing loss, linkage analysis, DFNB4, SLC26A4, Mutation.

Abstract: Deafness is the most common sensory disorder, which affects 1/1000 neonates globally



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