Association between a catechol-o-methyltransferase polymorphism and obsessive–compulsive disorder in the Afrikaner population
- 30 June 2001
- journal article
- research article
- Published by Elsevier in Journal of Affective Disorders
- Vol. 65 (1), 61-65
- https://doi.org/10.1016/s0165-0327(00)00246-9
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- The Origins of Hypertrophic Cardiomyopathy–Causing Mutations in Two South African Subpopulations: A Unique Profile of Both Independent and Founder EventsAmerican Journal of Human Genetics, 1999
- Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairsEuropean Journal of Human Genetics, 1999
- Identification of Genetic Markers Associated with Gilles de la Tourette Syndrome in an Afrikaner PopulationAmerican Journal of Human Genetics, 1998
- Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human GenomeScience, 1998
- Evidence of a long QT founder gene with varying phenotypic expression in South African families.Journal of Medical Genetics, 1996
- Kinetics of Human Soluble and Membrane-Bound Catechol O-Methyltransferase: A Revised Mechanism and Description of the Thermolabile Variant of the EnzymeBiochemistry, 1995
- A Molecular Investigation Suggests No Relationship between Obsessive-Compulsive Disorder and the Dopamine D2 ReceptorNeuropsychobiology, 1994
- The molecular basis and diagnosis of familial hypercholesterolaemia in South African AfrikanersAnnals of Human Genetics, 1991
- Obsessive-compulsive disorder: psychobiological approaches to diagnosis, treatment, and pathophysiologyBiological Psychiatry, 1987
- Erythrocyte catechol‐O‐methyltransferase activity in a Swedish populationClinical Genetics, 1981