PRRT2 gene mutations in familial and sporadic paroxysmal kinesigenic dyskinesia cases

Mov Disord. 2013 Aug;28(9):1313-4. doi: 10.1002/mds.25370. Epub 2013 Mar 1.
No abstract available

Publication types

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

MeSH terms

  • Asian People / genetics
  • Chorea / genetics*
  • Cohort Studies
  • Dystonia
  • Family Health*
  • Female
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Mutation / genetics*
  • Nerve Tissue Proteins / genetics*

Substances

  • Membrane Proteins
  • Nerve Tissue Proteins
  • PRRT2 protein, human

Supplementary concepts

  • Familial paroxysmal dystonia