A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in .

After is the second most common contributor to autosomal recessive nonsyndromic hearing loss (ARNSHL) worldwide. In this study, we used Exome Sequencing (ES) to present a village with 31 individuals affected by hereditary hearing loss (HHL) in southeastern Iran near the border of Pakistan. The village harbored the known pathogenic missense (NM_000441.