Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS

Neurology. 2011 Sep 13;77(11):1102-3. doi: 10.1212/WNL.0b013e31822e563c. Epub 2011 Aug 31.
No abstract available

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / genetics*
  • African Americans / genetics*
  • Aged
  • Amino Acid Sequence
  • Amyotrophic Lateral Sclerosis / diagnosis
  • Amyotrophic Lateral Sclerosis / genetics*
  • Cell Cycle Proteins / genetics*
  • Fatal Outcome
  • Female
  • Humans
  • Isoleucine / genetics*
  • Molecular Sequence Data
  • Mutation / genetics*
  • Valine / genetics*
  • Valosin Containing Protein

Substances

  • Cell Cycle Proteins
  • Isoleucine
  • Adenosine Triphosphatases
  • VCP protein, human
  • Valosin Containing Protein
  • Valine