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Volumn 10, Issue 12, 2005, Pages 1059-1061
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Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder
a,b,c b d e f g h a i f a j h b,c f d e b,k c d more.. |
Author keywords
[No Author keywords available]
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Indexed keywords
NEUROTRANSMITTER;
SEROTONIN;
SEROTONIN TRANSPORTER;
SEROTONIN UPTAKE INHIBITOR;
ALCOHOLISM;
ANOREXIA NERVOSA;
AUTISM;
CLINICAL STUDY;
DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS;
DISEASE PREDISPOSITION;
FAMILY HISTORY;
FATHER;
GENETIC POLYMORPHISM;
GENETIC RISK;
GENETIC TRANSCRIPTION;
GENETIC VARIABILITY;
GENOTYPE;
HUMAN;
LETTER;
OBSESSIVE COMPULSIVE DISORDER;
PHENOTYPE;
PHOBIA;
PRIORITY JOURNAL;
PROTEIN TRANSPORT;
SUICIDE;
TOBACCO DEPENDENCE;
ADOLESCENT;
ADULT;
ALCOHOLISM;
ANOREXIA NERVOSA;
CHILD;
CHILD DEVELOPMENT DISORDERS, PERVASIVE;
DRUG RESISTANCE;
FAMILY;
FEMALE;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
MALE;
MIDDLE AGED;
OBSESSIVE-COMPULSIVE DISORDER;
PEDIGREE;
POLYMORPHISM, GENETIC;
REFERENCE VALUES;
SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS;
SEROTONIN UPTAKE INHIBITORS;
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EID: 32844455970
PISSN: 13594184
EISSN: 14765578
Source Type: Journal
DOI: 10.1038/sj.mp.4001728 Document Type: Letter |
Times cited : (47)
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References (10)
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