Association between serotonergic candidate genes and specific phenotypes of obsessive compulsive disorder

Journal of Affective Disorders

Volumn 91, Issue 1, 2006, Pages 39-44

  Denys, Damiaan ^a,c   Van Nieuwerburgh, Filip ^b   Deforce, Dieter ^b   Westenberg, Herman G M ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b GHENT UNIVERSITY   (Belgium)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

Association studies; Genetics; Obsessive compulsive disorder; Serotonin

Indexed keywords

SEROTONIN 1B RECEPTOR; SEROTONIN 2A RECEPTOR; SEROTONIN TRANSPORTER;

ADULT; ALLELE; ARTICLE; COMORBIDITY; CONTROLLED STUDY; DNA POLYMORPHISM; FAMILY HISTORY; FEMALE; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; OBSESSIVE COMPULSIVE DISORDER; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL;

ADULT; ALLELES; CHROMOSOME DELETION; FEMALE; GENE FREQUENCY; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MUTAGENESIS, INSERTIONAL; OBSESSIVE-COMPULSIVE DISORDER; PHENOTYPE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; RECEPTOR, SEROTONIN, 5-HT1B; RECEPTOR, SEROTONIN, 5-HT2A; SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS; SEROTONIN UPTAKE INHIBITORS; TREATMENT OUTCOME;

EID: 32844473728     PISSN: 01650327     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jad.2005.12.011     Document Type: Article

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