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Novel Ferritin Light Chain Gene Mutation in a Korean Patient with Neuroferritinopathy

DC Field Value Language
dc.contributor.author류철형-
dc.date.accessioned2019-09-20T07:32:35Z-
dc.date.available2019-09-20T07:32:35Z-
dc.date.issued2019-
dc.identifier.issn2093-4939-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/170941-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherKorean Movement Disorders Society-
dc.relation.isPartOfJournal of Movement Disorders-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleNovel Ferritin Light Chain Gene Mutation in a Korean Patient with Neuroferritinopathy-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurology (신경과학교실)-
dc.contributor.googleauthorSo Hoon Yoon-
dc.contributor.googleauthorNan Young Kim-
dc.contributor.googleauthorYun Joong Kim-
dc.contributor.googleauthorChul Hyoung Lyoo-
dc.identifier.doi10.14802/jmd.18062-
dc.contributor.localIdA01333-
dc.relation.journalcodeJ01610-
dc.identifier.eissn2005-940X-
dc.identifier.pmid30732435-
dc.contributor.alternativeNameLyoo, Chul Hyoung-
dc.contributor.affiliatedAuthor류철형-
dc.citation.volume12-
dc.citation.number1-
dc.citation.startPage63-
dc.citation.endPage65-
dc.identifier.bibliographicCitationJournal of Movement Disorders, Vol.12(1) : 63-65, 2019-
dc.identifier.rimsid64365-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers

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