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

J Neurol Sci. 2020 Jul 15;414:116875. doi: 10.1016/j.jns.2020.116875. Epub 2020 May 1.
No abstract available

Keywords: HNRNPDL; IBM; Inclusion body myopathies; LGMD D3; Limb girdle muscle dystrophy; Myopathy.

Publication types

  • Letter

MeSH terms

  • Europe
  • Humans
  • Muscular Dystrophies, Limb-Girdle* / genetics
  • Phenotype