Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease

Adv Neurol. 1996:69:97-100.
No abstract available

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Base Sequence
  • Cytochrome P-450 CYP2D6
  • Cytochrome P-450 Enzyme System / genetics*
  • Cytochrome P-450 Enzyme System / metabolism
  • DNA / analysis
  • Debrisoquin / metabolism*
  • Female
  • Genotype
  • Heterozygote
  • Homozygote
  • Humans
  • Hydroxylation
  • Male
  • Mixed Function Oxygenases / genetics*
  • Mixed Function Oxygenases / metabolism
  • Molecular Sequence Data
  • Parkinson Disease / enzymology
  • Parkinson Disease / genetics*
  • Parkinson Disease / metabolism*
  • Polymorphism, Restriction Fragment Length

Substances

  • DNA
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • Cytochrome P-450 CYP2D6
  • Debrisoquin