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Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population
- Title
- Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population
- Author
- 고인송
- Keywords
- RTN4R; Schizophrenia; Single nucleotide polymorphism; EYE-MOVEMENT ABNORMALITY; POLYMORPHISMS
- Issue Date
- 2011-09
- Publisher
- ELSEVIER IRELAND LTD, ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000, IRELAND
- Citation
- Psychiatry Research, Vol.108, No.2 [2011], p312~314
- 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. (C) 2011 Elsevier Ltd. All rights reserved.
- URI
- http://www.psy-journal.com/article/S0165-1781(11)00098-9/fulltexthttp://www.sciencedirect.com/science/article/pii/S0165178111000989?via%3Dihub
- ISSN
- 0165-1781
- Appears in Collections:
- COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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