LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

Am J Hum Genet. 2005 Aug;77(2):330-2. doi: 10.1086/432422.
No abstract available

Publication types

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

MeSH terms

  • Africa, Northern
  • African Continental Ancestry Group
  • European Continental Ancestry Group
  • Family Health
  • Founder Effect*
  • Genetic Markers
  • Genotype
  • Haplotypes*
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Microsatellite Repeats
  • Middle Aged
  • Mutation*
  • Parkinson Disease / genetics*
  • Protein-Serine-Threonine Kinases / genetics*

Substances

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