LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease

Lancet Neurol. 2008 Jul;7(7):562-4. doi: 10.1016/S1474-4422(08)70118-2. Epub 2008 Jun 6.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Glycine / genetics
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Mutation / genetics
  • Parkinson Disease / classification*
  • Parkinson Disease / epidemiology
  • Parkinson Disease / genetics*
  • Protein-Serine-Threonine Kinases / genetics*
  • Serine / genetics

Substances

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