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Results 1 - 10 of 11 for Muscular "dystrophy," "limb-girdle," autosomal dominant 4
  1. ... DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12 MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, ...
  2. Muscular Dystrophy From the National Institutes of Health (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 ( ...
  3. ... Klepper J, Straub V. Does delta-sarcoglycan-associated autosomal-dominant ... muscular dystrophy-associated protein diseases. Neurologist. 2010 Nov;16(6): ...
  4. Limb-Girdle Muscular Dystrophy (LGMD) (Muscular Dystrophy Association)  
    Shoulder Injuries and Disorders/Related Issues ... Shoulder Injuries and Disorders ... Muscular Dystrophy/Specifics ... Muscular Dystrophy ... Muscular Dystrophy Association
  5. ... in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Hum Mol Genet. ...
  6. What Are the Types and Symptoms of Muscular Dystrophy (MD)? From the National Institutes of Health (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 ...
  7. ... 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 ...
  8. ... 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 ...
  9. ... as muscle cells. PABPN1 Most cases of oculopharyngeal muscular dystrophy are inherited in an autosomal dominant pattern, which means one copy of the altered ...
  10. ... 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. ...
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