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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
DOI
10.1016/j.psychres.2011.02.006
Appears in Collections:
COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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