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Late-onset vanishing white matter disease with compound heterozygous EIF2B5 gene mutations

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dc.contributor.authorLee, Ha-neul-
dc.contributor.authorKoh, Seong-Ho-
dc.contributor.authorLee, Kyu-Yong-
dc.contributor.authorKi, Chang-Seok-
dc.contributor.authorLee, Young Joo-
dc.date.accessioned2022-12-20T23:00:11Z-
dc.date.available2022-12-20T23:00:11Z-
dc.date.created2022-08-29-
dc.date.issued2009-03-
dc.identifier.issn1351-5101-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/177129-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-
dc.titleLate-onset vanishing white matter disease with compound heterozygous EIF2B5 gene mutations-
dc.typeArticle-
dc.contributor.affiliatedAuthorKoh, Seong-Ho-
dc.contributor.affiliatedAuthorLee, Kyu-Yong-
dc.contributor.affiliatedAuthorLee, Young Joo-
dc.identifier.doi10.1111/j.1468-1331.2008.02395.x-
dc.identifier.scopusid2-s2.0-60049098370-
dc.identifier.wosid000263133500002-
dc.identifier.bibliographicCitationEUROPEAN JOURNAL OF NEUROLOGY, v.16, no.3, pp.e42 - e43-
dc.relation.isPartOfEUROPEAN JOURNAL OF NEUROLOGY-
dc.citation.titleEUROPEAN JOURNAL OF NEUROLOGY-
dc.citation.volume16-
dc.citation.number3-
dc.citation.startPagee42-
dc.citation.endPagee43-
dc.type.rimsART-
dc.type.docTypeLetter-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusLEUKOENCEPHALOPATHY-
dc.subject.keywordAuthoradult-onset vanishing white matter disease-
dc.subject.keywordAuthordementia-
dc.subject.keywordAuthorgait disturbance-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1111/j.1468-1331.2008.02395.x-
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