Article

Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach

2020-09-23

Abstract excerpt

<h4>ABSTRACT</h4> <h4>Background</h4> Hearing loss is one of the most common birth disorders in humans with an estimated prevalence of 1-3 in every 1000 newborns. This study has investigated the molecular etiology of a deaf cohort using a stepwise strategy to effectively diagnose patients and the challenges faced to verify genetic heterogenicity and the variable mutation spectrums of hearing loss. <h4>Methods</h4>...

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Literature Corpus work: 7b51bdfb-b72d-52fb-99a9-e74fcb304789
DOI: 10.1101/2020.09.20.20197145

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