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