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Author Spotlight: Optimizing EAS with Long Electrodes for Enhanced Cochlear Coverage and Hearing Preservation
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Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic

Maliheh Alimardani1,2,3, Seyed Mojtaba Hosseini3,4, Mahmoud Shekari Khaniani2,5

  • 1a Neurosciences Research Center , Tabriz University of Medical Science , Tabriz , Iran.

Fetal and Pediatric Pathology
|December 25, 2018
PubMed
Abstract

Keywords:
CDH23Iranian populationMYO6PJVKSLC26A4nonsyndromic hearing loss

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