LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease

Clin Genet. 2007 Apr;71(4):367-70. doi: 10.1111/j.1399-0004.2007.00771.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Case-Control Studies
  • Female
  • Genes, Dominant
  • Haplotypes
  • Heterozygote
  • Humans
  • Italy
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Male
  • Middle Aged
  • Parkinson Disease / genetics*
  • Point Mutation*
  • Protein Serine-Threonine Kinases / genetics*

Substances

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