Management of congenital muscular dystrophies related to defects in the LMNA gene

Abstract

Congenital Muscular Dystrophies are a heterogeneous group of muscular disorders defined as early onset muscle weakness and progressive course associated to dystrophic features at muscle biopsy. CMDs related to lamina A/C gene (LMNA) defect include different phenotypes that can be classified as i) severe phenotype with generalized muscular weakness and… (More)

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