Results 1 -
10
of
11
for
Muscular "dystrophy," "limb-girdle," autosomal dominant 4
- ... DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12 MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, ...
- Muscular Dystrophy (National Institute of Neurological Disorders and Stroke)Muscular Dystrophy/Start Here ... Muscular Dystrophy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Muscular dystrophy ( ...
- ... Klepper J, Straub V. Does delta-sarcoglycan-associated autosomal-dominant ... muscular dystrophy-associated protein diseases. Neurologist. 2010 Nov;16(6): ...
- Limb-Girdle Muscular Dystrophy (LGMD) (Muscular Dystrophy Association)Muscular Dystrophy/Specifics ... Muscular Dystrophy ... Shoulder Injuries and Disorders/Related Issues ... Shoulder Injuries and Disorders ... Muscular Dystrophy Association
- ... in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Hum Mol Genet. ...
- What Are the Types and Symptoms of Muscular Dystrophy (MD)? (Eunice Kennedy Shriver National Institute of Child Health and Human Development)Muscular Dystrophy/Specifics ... Muscular Dystrophy ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes ...
- ... cause other caveolinopathies including CAV3-related distal myopathy, limb-girdle muscular dystrophy, ... This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... CAV3 gene mutations can cause other caveolinopathies including limb-girdle muscular dystrophy, ... This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... as muscle cells. PABPN1 Most cases of oculopharyngeal muscular dystrophy are inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... Lisanti MP. Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases. Neurology. 2004 Feb 24;62(4):538-43. doi: 10.1212/wnl.62.4. ...