Structural variants in the vesicular monoamine transporter do not contribute to sporadic Parkinson's disease

Mov Disord. 2006 Mar;21(3):426-7. doi: 10.1002/mds.20798.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Exons / genetics
  • Female
  • Humans
  • Male
  • Mass Screening / methods
  • Middle Aged
  • Parkinson Disease / epidemiology
  • Parkinson Disease / genetics
  • Parkinson Disease / metabolism*
  • Periodicity*
  • Vesicular Monoamine Transport Proteins / genetics
  • Vesicular Monoamine Transport Proteins / metabolism*

Substances

  • SLC18A2 protein, human
  • Vesicular Monoamine Transport Proteins