Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease.

Santt, O; Baranova, H; Albuisson, E; Bignon, Y-J; Lucotte, G

Santt, O; Baranova, H; Albuisson, E; Bignon, Y-J; Lucotte, G.

Affiliation

Santt O; Center of Molecular Neurogenetics, Paris, France.

Eur J Neurol ; 11(4): 247-51, 2004 Apr.

Article in En | MEDLINE | ID: mdl-15061826

Subject(s)

Alleles; Cytochrome P-450 CYP2D6/deficiency; Glutathione Transferase/genetics; Parkinson Disease/genetics; Adult; Aged; Aged, 80 and over; Blotting, Southern/methods; Case-Control Studies; Cytochrome P-450 CYP2D6/genetics; Cytochrome P-450 CYP2D6/metabolism; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Odds Ratio; Polymerase Chain Reaction/methods; Polymorphism, Restriction Fragment Length

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Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Cytochrome P-450 CYP2D6 / Alleles / Glutathione Transferase Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2004 Document type: Article Affiliation country: France Country of publication: United kingdom

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