Role of selected mutations in exon 28 and 39 of Myosin15 gene in autosomal recessive nonsyndromic sensorineural deafness among affected South Indian families

High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India

“…Initially, we checked for the reported mutations of Myosin 15 gene (in exon 28 and exon39) in this population. We could not detect any of the reported mutations [16].…”