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

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dc.contributor.authorPasaje, Charisse Flerida A.-
dc.contributor.authorBae, Joon Seol-
dc.contributor.authorPark, Byung-Lae-
dc.contributor.authorPark, Chul Soo-
dc.contributor.authorKim, Bong-Jo-
dc.contributor.authorLee, Cheol-Soon-
dc.contributor.authorKim, Jae Won-
dc.contributor.authorChoi, Woo Hyuk-
dc.contributor.authorShin, Tae-Min-
dc.contributor.authorKoh, In Song-
dc.contributor.authorChoi, Ihn-Geun-
dc.contributor.authorWoo, Sung-Il-
dc.contributor.authorShin, Hyoung Doo-
dc.date.accessioned2022-07-16T19:15:08Z-
dc.date.available2022-07-16T19:15:08Z-
dc.date.issued2011-09-
dc.identifier.issn0165-1781-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/167705-
dc.description.abstractThis 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.-
dc.format.extent3-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleLack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population-
dc.typeArticle-
dc.publisher.location아일랜드-
dc.identifier.doi10.1016/j.psychres.2011.02.006-
dc.identifier.scopusid2-s2.0-80052793169-
dc.identifier.wosid000295748200026-
dc.identifier.bibliographicCitationPsychiatry Research, v.189, no.2, pp 312 - 314-
dc.citation.titlePsychiatry Research-
dc.citation.volume189-
dc.citation.number2-
dc.citation.startPage312-
dc.citation.endPage314-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassssci-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPsychiatry-
dc.relation.journalWebOfScienceCategoryPsychiatry-
dc.subject.keywordPlusEYE-MOVEMENT ABNORMALITY-
dc.subject.keywordPlusPOLYMORPHISMS-
dc.subject.keywordAuthorRTN4R-
dc.subject.keywordAuthorSchizophrenia-
dc.subject.keywordAuthorSingle nucleotide polymorphism-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0165178111000989?via%3Dihub-
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