MYH6(redirected from ASD3)
MYH6A gene on chromosome 14q12 that encodes a heavy chain of myosin and is thus involved in cytokinesis, cell shape and specialised functions—e.g., secretion and capping.
MYH6 mutation causes familial hypertrophic cardiomyopathy and atrial septal defect 3.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.