MYO15A and deafness: Three mutations, c.3971C>A (p.A1324D), c.4011insA (p.Q1337Qfs∗22), and c.9690+1G>A, were detected in MYO15A gene (NM_016239), which were cosegregated with the disease, suggesting that these mutations may be the etiology of deafness in this ARNSHL family.