Condition: Deafness, autosomal dominant nonsyndromic sensorineural 22


rs121912560 in MYO6 gene and Deafness, autosomal dominant nonsyndromic sensorineural 22 PMID 15060111 2004 Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).