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Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population
- Authors
- Pasaje, Charisse Flerida A.; Bae, Joon Seol; Park, Byung-Lae; Park, Chul Soo; Kim, Bong-Jo; Lee, Cheol-Soon; Kim, Jae Won; Choi, Woo Hyuk; Shin, Tae-Min; Koh, In Song; Choi, Ihn-Geun; Woo, Sung-Il; Shin, Hyoung Doo
- Issue Date
- 30-Sep-2011
- Publisher
- Elsevier BV
- Keywords
- RTN4R; Schizophrenia; Single nucleotide polymorphism
- Citation
- Psychiatry Research, v.189, no.2, pp 312 - 314
- Pages
- 3
- Journal Title
- Psychiatry Research
- Volume
- 189
- Number
- 2
- Start Page
- 312
- End Page
- 314
- ISSN
- 0165-1781
- 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.
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Related Researcher
- WOO, SUNG IL
- College of Medicine (Department of Psychiatry)