Eye movement disorders in ATP13A2 mutation carriers (PARK9)

Mov Disord. 2010 Nov 15;25(15):2687-9. doi: 10.1002/mds.23352.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Chile
  • Eye Movement Measurements
  • Eye Movements / genetics*
  • Female
  • Heterozygote
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Ocular Motility Disorders / genetics*
  • Proton-Translocating ATPases / genetics*

Substances

  • ATP13A2 protein, human
  • Proton-Translocating ATPases