Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain

Mov Disord. 2013 Feb;28(2):248. doi: 10.1002/mds.25293. Epub 2013 Feb 6.
No abstract available

Publication types

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

MeSH terms

  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Haplotypes
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Mutation, Missense / genetics*
  • Parkinson Disease / epidemiology*
  • Parkinson Disease / genetics*
  • Protein Serine-Threonine Kinases / genetics*
  • South America / epidemiology
  • Spain / epidemiology

Substances

  • LRRK2 protein, human
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Protein Serine-Threonine Kinases