Article
Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles.
Biological psychiatry - 15 Aug 1999
Palmatier M A, Kang A M, Kidd K K
Abstract excerpt
BACKGROUND: Catechol-O-methyltransferase (COMT) has been investigated as a candidate gene in many neurologic disorders involving catecholaminergic systems. The NlaIII restriction site polymorphism (RSP) at COMT is a G<-->A (site absent<-->site present) single nucleotide polymorphism (SNP) at nucleotide 322/472 (in the short or long mRNA) that results in a Val<-->Met polymorphism at amino acid 108/158 (in soluble...
Topics
- Alleles
- Animals
- Catechol O-Methyltransferase
- Central Nervous System Diseases
- Female
- Gene Frequency
- Genetic Linkage
- Genetic Markers
- Humans
- Male
- Mental Disorders
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Primates
- Racial Groups
- Reference Values
