LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs

N Engl J Med. 2006 Jan 26;354(4):422-3. doi: 10.1056/NEJMc055540.
No abstract available

Publication types

  • Letter

MeSH terms

  • Africa, Northern / ethnology
  • Arabs / genetics*
  • Heterozygote
  • Homozygote
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Middle Aged
  • Mutation
  • Parkinson Disease / genetics*
  • Protein-Serine-Threonine Kinases / genetics*

Substances

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