Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation

Neurology. 2008 Apr 15;70(16 Pt 2):1501-3. doi: 10.1212/01.wnl.0000310431.41036.e0.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • Deep Brain Stimulation* / methods
  • Dystonia / complications
  • Dystonia / genetics*
  • Dystonia / therapy
  • Humans
  • Male
  • Mutation / genetics*
  • Parkinsonian Disorders / complications
  • Parkinsonian Disorders / genetics*
  • Parkinsonian Disorders / therapy
  • Sodium-Potassium-Exchanging ATPase / genetics*

Substances

  • ATP1A3 protein, human
  • Sodium-Potassium-Exchanging ATPase