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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
- Sep-2011
- Publisher
- Elsevier BV
- Keywords
- RTN4R; Schizophrenia; Single nucleotide polymorphism
- Citation
- Psychiatry Research, v.189, no.2, pp 312 - 314
- Pages
- 3
- Indexed
- SCI
SCIE
SSCI
SCOPUS
- 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.
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