Association study of NlaIII and MspI genetic polymorphisms of catechol-O-methyltransferase gene and susceptibility to Schizophrenia
- 1 May 1997
- journal article
- research article
- Published by Elsevier in Biological Psychiatry
- Vol. 41 (9) , 985-987
- https://doi.org/10.1016/s0006-3223(97)00045-0
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- The Future of Genetic Studies of Complex Human DiseasesScience, 1996
- No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activityAmerican Journal of Psychiatry, 1996
- Potential linkage for schizophrenia on chromosome 22q12‐q13: A replication studyAmerican Journal of Medical Genetics, 1995
- Follow‐up report of potential linkage for schizophrenia on chromosome 22q: Part 3American 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
- Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q11American Journal of Medical Genetics, 1993
- The human catechol-O-methyltransferase (COMT) gene maps to band q11.2 of chromosome 22 and shows a frequent RFLP with BglICytogenetic and Genome Research, 1992
- Late‐Onset psychosis in the velo‐cardio‐facial syndromeAmerican Journal of Medical Genetics, 1992
- S-adenosylmethionine and Catechol-O-methyltransferase in SchizophreniaAmerican Journal of Psychiatry, 1972
- Current Biochemical Approaches to SchizophreniaNew England Journal of Medicine, 1967