Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*

Brain. 2005 Dec;128(Pt 12):3000-11. doi: 10.1093/brain/awh666.
No abstract available

MeSH terms

  • Adult
  • Brain / pathology
  • Case-Control Studies
  • DNA Mutational Analysis
  • DNA Primers
  • Echoencephalography
  • Exons
  • Female
  • Genes, Dominant*
  • Haplotypes
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Mutation, Missense / genetics*
  • Neuropsychological Tests
  • Parkinson Disease / diagnostic imaging
  • Parkinson Disease / genetics*
  • Parkinson Disease / pathology
  • Pedigree
  • Penetrance
  • Protein Serine-Threonine Kinases / genetics*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

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