HAL (France)
open access
Natural history of LGMD2A for delineating outcome measures in clinical trials
Objective Limb-girdle muscular dystophy 2A (LGMD2A, OMIM) is a slowly progressive myopathy caused by the deficiency in calpain 3, a calcium-dependent cysteine protease of the skeletal muscle. Methods In this study, we carried out an observational study of clinical manifestations and disease progress
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