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

AuthorsR Bordet, F Broly, A Destée, C Libersa
JournalAdvances in neurology (Adv Neurol) Vol. 69 Pg. 97-100 ( 1996) ISSN: 0091-3952 [Print] United States
PMID8615190 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • DNA
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • Cytochrome P-450 CYP2D6
  • Debrisoquin
Topics
  • Aged
  • Base Sequence
  • Cytochrome P-450 CYP2D6
  • Cytochrome P-450 Enzyme System (genetics, metabolism)
  • DNA (analysis)
  • Debrisoquin (metabolism)
  • Female
  • Genotype
  • Heterozygote
  • Homozygote
  • Humans
  • Hydroxylation
  • Male
  • Mixed Function Oxygenases (genetics, metabolism)
  • Molecular Sequence Data
  • Parkinson Disease (enzymology, genetics, metabolism)
  • Polymorphism, Restriction Fragment Length

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