CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

Author:

Planté-Bordeneuve V.,Bandmann O.,Wenning G.,Quinn N. P.,Daniel S. E.,Harding A. E.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference10 articles.

1. Identification of the primary gene defect at the cytochrome P450 CYP2D6 locus;Gough;Nature,1990

2. The human CYP2D6 locus associated with a common genetic defect in drug oxidation: a G1943 to A base change in intron 3 of a mutant CYP2D6 allele results in an aberrant 3′ recognition site;Hanioka;Am J Hum Genet,1990

3. Deletion of the entire CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism;Gaedigk;Am J Hum Genet,1991

4. Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine;Barbeau;Lancet,1985

5. Oxidative polymorphism of debrisoquine in Parkinson's disease;Benitez;J Neurol Neurosurg Psychiatry,1990

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4. Genetic Variants of the α-Synuclein Gene SNCA Are Associated with Multiple System Atrophy;PLoS ONE;2009-09-22

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