Rashidi, Fatemeh Sadat <br/><br/>
Association of the functional serotonin transporter haplotype with familial form of obsessive compulsive disorder in Iranian patients.  [electronic resource] 

 -  International journal of psychiatry in clinical practice  Mar 2018 
 - 47-53 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1471-1788 
<br/><br/><label>Standard No.: </label>10.1080/13651501.2017.1353634  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Female<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Haplotypes<br/>Humans<br/>Iran<br/>Male<br/>Middle Aged<br/>Obsessive-Compulsive Disorder--genetics<br/>Polymorphism, Single Nucleotide<br/>Serotonin Plasma Membrane Transport Proteins--genetics