Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia

Neuromuscul Disord. 2015 Mar;25(3):273. doi: 10.1016/j.nmd.2014.10.007. Epub 2014 Oct 24.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Adenosine Triphosphatases / genetics*
  • Cell Cycle Proteins / genetics*
  • Female
  • Frontotemporal Dementia / genetics*
  • Humans
  • Male
  • Muscular Dystrophies, Limb-Girdle / genetics*
  • Mutation / genetics*
  • Myositis, Inclusion Body / genetics*
  • Osteitis Deformans / genetics*

Substances

  • Cell Cycle Proteins
  • Adenosine Triphosphatases