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Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population.
- Source :
-
Psychiatry research [Psychiatry Res] 2011 Sep 30; Vol. 189 (2), pp. 312-4. Date of Electronic Publication: 2011 Mar 05. - Publication Year :
- 2011
-
Abstract
- This study examined the association of the reticulon 4 receptor (RTN4R) gene with schizophrenia and smooth pursuit eye movement (SPEM) abnormality in a Korean population. Although we failed to provide convincing evidence that RTN4R is associated with schizophrenia development and SPEM impairment, our findings may be useful for further genetic studies.<br /> (Copyright © 2011 Elsevier Ltd. All rights reserved.)
- Subjects :
- Electrooculography methods
Female
GPI-Linked Proteins genetics
Genetic Predisposition to Disease genetics
Genome-Wide Association Study
Humans
Male
Nogo Receptor 1
Regression Analysis
Republic of Korea
Risk Factors
Myelin Proteins genetics
Ocular Motility Disorders genetics
Polymorphism, Single Nucleotide genetics
Pursuit, Smooth genetics
Receptors, Cell Surface genetics
Schizophrenia genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0165-1781
- Volume :
- 189
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Psychiatry research
- Publication Type :
- Academic Journal
- Accession number :
- 21377214
- Full Text :
- https://doi.org/10.1016/j.psychres.2011.02.006