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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15

A M Waryah1, A Rehman, Z M Ahmed

  • 1National Centre of Excellence in Molecular Biology, Punjab University, Lahore 53700, Pakistan.

Clinical Genetics
|August 5, 2009
PubMed

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