Cytochrome P450 2E1 gene polymorphisms/haplotypes and Parkinson’s disease in a Swedish population

Author:

Niazi Shahabi H.,Westberg L.,Melke J.,Håkansson A.,Belin A. Carmine,Sydow O.,Olson L.,Holmberg B.,Nissbrandt H.

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Psychiatry and Mental health,Clinical Neurology,Neurology

Reference51 articles.

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2. Bandmann O, Vaughan J, Holmans P, Marsden CD, Wood NW (1997) Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson’s disease. Lancet 350(9085):1136–1139

3. Brockmoller J, Cascorbi I, Kerb R, Roots I (1996) Combined analysis of inherited polymorphisms in arylamine N-acetyltransferase 2, glutathione S-transferases M1 and T1, microsomal epoxide hydrolase, and cytochrome P450 enzymes as modulators of bladder cancer risk. Cancer Res 56(17):3915–3925

4. Brzezinski MR, Boutelet-Bochan H, Person RE, Fantel AG, Juchau MR (1999) Catalytic activity and quantitation of cytochrome P-450 2E1 in prenatal human brain. J Pharmacol Exp Ther 289(3):1648–1653

5. Carriere V, Berthou F, Baird S, Belloc C, Beaune P, de Waziers I (1996) Human cytochrome P450 2E1 (CYP2E1): from genotype to phenotype. Pharmacogenetics 6(3):203–211

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