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Article

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

Advances in neurology - 1 Jan 1996

Bordet R, Broly F, Destée A, Libersa C

Abstract excerpt

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Share to Cytochrome P-450 CYP2D6
Share to Cytochrome P-450 Enzyme System
Share to Debrisoquin
Share to Homozygote

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hydroxylation

Share to Mixed Function Oxygenases

Share to Parkinson Disease

Share to Polymorphism, Restriction Fragment Length

Source

Identifiers

PMID: 8615190

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.PMID 8615190Read ↗

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Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease.Semantic proximity Read ↗

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Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonism.Semantic proximity Read ↗

Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families.Semantic proximity Read ↗

Pharmacogenetics of Debrisoquine and its Use as a Marker For CYP2D6 Hydroxylation CapacitySemantic proximity Read ↗

The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease.Semantic proximity Read ↗

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.Semantic proximity Read ↗

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Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease.Semantic proximity Read ↗

Debrisoquine oxidation in Parkinson's disease.Semantic proximity Read ↗

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