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

Fatemeh Sadat Rashidi; Ehsan Ahmadipour; Sepideh Shiravand; Abolhassan Ahmadiani; Sareh Asadi; Jamal Shams

doi:10.1080/13651501.2017.1353634

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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.

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. This record was last updated on 06/09/2018 and may not reflect the most current and accurate biomedical/scientific data available from NLM. The corresponding record at NLM can be accessed at https://www.ncbi.nlm.nih.gov/pubmed/28691545

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