Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia
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Limb-girdle muscular dystrophy (LGMD) type 2A (calpainopathy) is an autosomal recessive disease caused by mutation in the CAPN3 gene. The aim of this study was to examine genetic and phenotypic features of Serbian patients with calpainopathy. The study compris... ...
