Symptoms of B4GAT1 Gene Muscular Dystrophy-Dystroglycanopathy Congenital with Brain and Eye Anomalies Type A13 Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies, also known as Type A13, is a rare genetic disorder caused by mutations in the B4GAT1 gene. This condition is part of a group of diseases known as limb-girdle muscular dystrophies, which are […]
