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American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 96, Issue 6, 2000, Pages 721-724

Association between homozygosty at the COMT gene locus and obsessive compulsive disorder

(5) Schindler, Kim M a Richter, M A b Kennedy, James L b Pato, Michele T a Pato, Carlos N a,c

a UNIVERSITY AT BUFFALO (United States)

b UNIVERSITY OF TORONTO (Canada)

c UNIVERSITY AT BUFFALO (United States)

Author keywords

Candidate gene; Haplotype relative risk; OCD; Transmission disequilibrium

Indexed keywords

CATECHOL METHYLTRANSFERASE; DNA;

ADULT; ALLELE; ARTICLE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENOTYPE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; OBSESSION; POPULATION GENETICS; PRIORITY JOURNAL; SEX DIFFERENCE; ENZYMOLOGY; GENETICS; HOMOZYGOTE; OBSESSIVE COMPULSIVE DISORDER;

BUBALUS;

ALLELES; CATECHOL O-METHYLTRANSFERASE; DNA; FEMALE; GENE FREQUENCY; GENOTYPE; HOMOZYGOTE; HUMANS; MALE; OBSESSIVE-COMPULSIVE DISORDER;

EID: 0034606203 PISSN: 15524841 EISSN: 1552485X Source Type: Journal
DOI: None Document Type: Article

Times cited : (64)

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