Condition: Deafness, Autosomal Dominant 11


rs121965084 in MYO7A gene and Deafness, Autosomal Dominant 11 PMID 15300860 2004 Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11).

PMID 15121790 2004 Modifier controls severity of a novel dominant low-frequency MyosinVIIA (MYO7A) auditory mutation.

PMID 9354784 1997 Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.

PMID 15221449 2004 Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).