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"Limb-girdle" muscular "dystrophy," type 2A
- ... CAPN3 gene have been identified in people with limb-girdle muscular dystrophy type 2A. This form of limb-girdle muscular dystrophy is ... Spencer MJ. Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A). Biochim Biophys Acta. 2007 Feb;1772(2):128- ...
- ... an inheritance pattern called autosomal recessive.Calpainopathy, or limb-girdle muscular dystrophy type 2A, is caused by mutations in the CAPN3 gene. ...
- ... F, Stanoiu B, Zavaleanu M. Merosin-deficient congenital muscular dystrophy type 1A. ... of limb-girdle muscular dystrophy due to LAMA2 mutations. Muscle Nerve. ...