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Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population
- Pasaje, Charisse Flerida A.;
- Bae, Joon Seol;
- Park, Byung-Lae;
- Park, Chul Soo;
- Kim, Bong-Jo;
- ... Shin, Hyoung Doo;
- 외 7명
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3초록
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.
키워드
RTN4R; Schizophrenia; Single nucleotide polymorphism; EYE-MOVEMENT ABNORMALITY; POLYMORPHISMS
- 제목
- Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population
- 저자
- 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
- 발행일
- 2011-09-30
- 유형
- Article
- 권
- 189
- 호
- 2
- 페이지
- 312 ~ 314
- 언어
- ENG
- 출판사
- Elsevier BV
- 발행국가
- 아일랜드
- 분량
- 3 페이지
- ISSN
- P 0165-1781