Severe limb-girdle muscular dystrophy 2A in two young siblings from Guinea-Bissau associated with a novel null homozygous mutation in CAPN3 gene.

Journal: Neuromuscular disorders : NMD

Publication date: 2019

Journal: Neuromuscular disorders : NMD

Publication Year: 2019

Authors & Co-authors:  Oliveira Santos Miguel M Ninitas Pedro P Conceição Isabel I