High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease
- 1 January 1997
- journal article
- clinical trial
- Published by Elsevier in Neuroscience Letters
- Vol. 221 (2-3) , 202-204
- https://doi.org/10.1016/s0304-3940(96)13289-4
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- No association between Parkinson's disease and monoamine oxidase A and B gene polymorphismsNeuroscience Letters, 1996
- Association analysis of a polymorphism of the monoamine oxidase B gene with Parkinson's disease in a Japanese populationAmerican Journal of Medical Genetics, 1995
- Kinetics of Human Soluble and Membrane-Bound Catechol O-Methyltransferase: A Revised Mechanism and Description of the Thermolabile Variant of the EnzymeBiochemistry, 1995
- Association of a monoamine oxidase B allele with Parkinson's diseaseAnnals of Neurology, 1993
- Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's diseaseThe Lancet, 1992
- Mutant debrisoquine hydroxylation genes in Parkinson's diseaseThe Lancet, 1992
- Cloning and Characterization of Human Placental Catechol--Methyltransferase cDNADNA and Cell Biology, 1991
- Epidemiology of Parkinson’s disease-interplaying genes and environmental factorsPublished by Springer Nature ,1991
- Chronic Parkinsonism in Humans Due to a Product of Meperidine-Analog SynthesisScience, 1983
- Erythrocyte catechol‐O‐methyltransferase activity in a Swedish populationClinical Genetics, 1981