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Association of the functional serotonin transporter haplotype with familial form of obsessive compulsive disorder in Iranian patients.

Authors
  • Rashidi, Fatemeh Sadat1
  • Ahmadipour, Ehsan1
  • Shiravand, Sepideh1
  • Ahmadiani, Abolhassan1
  • Asadi, Sareh2
  • Shams, Jamal3
  • 1 a Neuroscience Research Center , Shahid Beheshti University of Medical Sciences , Tehran , Iran. , (Iran)
  • 2 b NeuroBiology Research Center , Shahid Beheshti University of Medical Sciences , Tehran , Iran. , (Iran)
  • 3 c Behavioral Sciences Research Center , Shahid Beheshti University of Medical Science , Tehran , Iran. , (Iran)
Type
Published Article
Journal
International journal of psychiatry in clinical practice
Publication Date
Aug 11, 2017
Pages
1–7
Identifiers
DOI: 10.1080/13651501.2017.1353634
PMID: 28691545
Source
Medline
Keywords
License
Unknown

Abstract

The findings of this study showed the association of SLC6A4 variants with familial form of OCD and proposed stratified analyses in the genetic studies facilitate identification of genetic risk factors for this heterogeneous disorder.

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