5HT1Dβ receptor gene implicated in the pathogenesis of obsessive-compulsive disorder: Further evidence from a family-based association study

Molecular Psychiatry

Volumn 7, Issue 7, 2002, Pages 805-809

  Mundo, E ^a   Richter, M A ^a   Zai, G ^a   Sam, F ^a   McBride, J ^a   Macciardi, F ^a   Kennedy, James L ^a  

^a UNIVERSITY OF TORONTO   (Canada)

Author keywords

5HT1D ; Family based association test; Genetics; Linkage disequilibrium; Obsessive Compulsive Disorder; Quantitative traits; Receptor gene

Indexed keywords

RECEPTOR SUBTYPE; SEROTONIN 1D RECEPTOR; SEROTONIN RECEPTOR;

ADULT; ALLELE; ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; FAMILY STUDY; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MARKER GENE; OBSESSION; ONSET AGE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; QUANTITATIVE TRAIT; SAMPLE SIZE; SYMPTOM; FAMILY HEALTH; GENETICS; OBSESSIVE COMPULSIVE DISORDER;

FAMILY HEALTH; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; OBSESSIVE-COMPULSIVE DISORDER; RECEPTOR, SEROTONIN, 5-HT1D; RECEPTORS, SEROTONIN;

EID: 0036025372     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4001059     Document Type: Article

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