Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.
Identifieur interne : 001D96 ( Ncbi/Curation ); précédent : 001D95; suivant : 001D97Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.
Auteurs : R. Bordet [France] ; F. Broly ; A. Destée ; C. LibersaSource :
- Advances in neurology [ 0091-3952 ] ; 1996.
English descriptors
- KwdEn :
- 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.
- MESH :
- chemical , analysis : DNA.
- chemical , genetics : Cytochrome P-450 Enzyme System, Mixed Function Oxygenases.
- chemical , metabolism : Cytochrome P-450 Enzyme System, Debrisoquin, Mixed Function Oxygenases.
- chemical : Cytochrome P-450 CYP2D6.
- enzymology : Parkinson Disease.
- genetics : Parkinson Disease.
- metabolism : Parkinson Disease.
- Aged, Base Sequence, Female, Genotype, Heterozygote, Homozygote, Humans, Hydroxylation, Male, Molecular Sequence Data, Polymorphism, Restriction Fragment Length.
PubMed: 8615190
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pubmed:8615190Le document en format XML
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