HNRNPDL-related limb girdle muscular dystrophy in a Spanish family with scapulo-peroneal phenotype, the first family in Europe.

(Journal of the neurological sciences, v414:116875)
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TitleHNRNPDL-related limb girdle muscular dystrophy in a Spanish family with scapulo-peroneal phenotype, the first family in Europe.
Date2020-07-15
Issue nameJournal of the neurological sciences
Issue numberv414:116875
DOI10.1016/j.jns.2020.116875
PubMed32407983
AuthorsVicente LM, Martí P, Azorín I, Olivé M, Muelas N & Vilchez JJ
KeywordsHNRNPDL, IBM, Inclusion body myopathies, LGMD D3, Limb girdle muscle dystrophy, Myopathy
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