Delorme, R <br/><br/>
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.  [electronic resource] 

 -  Molecular psychiatry  Dec 2005 
 - 1059-61 p.  digital 
<br/><br/> Publication Type: Clinical Trial; Comparative Study; Letter 
<br/><br/><label>ISSN: </label>1359-4184 
<br/><br/><label>Standard No.: </label>10.1038/sj.mp.4001728  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alcoholism--genetics<br/>Anorexia Nervosa--genetics<br/>Child<br/>Child Development Disorders, Pervasive--genetics<br/>Drug Resistance--genetics<br/>Family<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Obsessive-Compulsive Disorder--drug therapy<br/>Pedigree<br/>Polymorphism, Genetic--genetics<br/>Reference Values<br/>Serotonin Plasma Membrane Transport Proteins--genetics<br/>Selective Serotonin Reuptake Inhibitors--therapeutic use