Detection and Analysis of Four Polymorphic Markers at the Human Monoamine Oxidase (MAO) Gene in Japanese Controls and Patients with Parkinson's Disease
- 18 June 1998
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 247 (2) , 452-456
- https://doi.org/10.1006/bbrc.1998.8812
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- G/A1947 polymorphism in catechol‐O‐methyltransferase (COMT) gene in Parkinson's diseaseMovement Disorders, 1997
- How far are we in understanding the cause of Parkinson's disease?Journal of Neurology, Neurosurgery & Psychiatry, 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
- Hereditary variations in monoamine oxidase as a risk factor for Parkinson's diseaseMovement Disorders, 1994
- Dopamine D3 and D4 receptor gene polymorphisms and Parkinson's diseaseThe Lancet, 1993
- Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motifGenomics, 1992
- Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB geneGenomics, 1992
- Detection and characterization of additional DNA polymorphisms in the dopamine D2 receptor geneGenomics, 1991
- Platelet and plasma amine oxidase activity in 680 normals: Sex and age differences and stability over timeBiochemical Medicine, 1976
- Standard calculations for evaluating a blood-group systemHeredity, 1951