Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population

Autor:	Chul-Soo Park, Hyoung Doo Shin, Jae Won Kim, Ihn-Geun Choi, Woo Hyuk Choi, In Song Koh, Cheol-Soon Lee, Bong-Jo Kim, Sung-ll Woo, Byung-Lae Park, Charisse Flerida A. Pasaje, Tae-Min Shin, Joon Seol Bae
Rok vydání:	2011
Předmět:	Male genetic structures Receptors Cell Surface Single-nucleotide polymorphism GPI-Linked Proteins Bioinformatics Polymorphism Single Nucleotide Smooth pursuit Ocular Motility Disorders Risk Factors Nogo Receptor 1 Republic of Korea mental disorders Genetic variation medicine Humans Genetic Predisposition to Disease Association (psychology) Biological Psychiatry Genetics Korean population business.industry medicine.disease Pursuit Smooth Reticulon 4 receptor Electrooculography Psychiatry and Mental health Schizophrenia Regression Analysis Female Abnormality business Myelin Proteins Genome-Wide Association Study
Zdroj:	Psychiatry Research. 189:312-314
ISSN:	0165-1781
DOI:	10.1016/j.psychres.2011.02.006
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f533edbf17e17cac9b700a5f49b9d23 https://doi.org/10.1016/j.psychres.2011.02.006 Zobrazit plný text záznamu Full Text from ScienceDirect