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Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia

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dc.contributor.author지민진-
dc.contributor.author정성원-
dc.contributor.author서하은-
dc.contributor.author김우람-
dc.contributor.author김소라-
dc.contributor.author이진숙-
dc.contributor.author노영-
dc.date.available2020-05-12T11:43:05Z-
dc.date.created2020-04-16-
dc.date.issued2020-04-
dc.identifier.issn1738-6586-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/41938-
dc.language영어-
dc.language.isoen-
dc.publisher대한신경과학회-
dc.relation.isPartOfJournal of Clinical Neurology-
dc.titleHeterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia-
dc.title.alternativeHeterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000527858700028-
dc.identifier.bibliographicCitationJournal of Clinical Neurology, v.16, no.2, pp.352 - 354-
dc.identifier.kciidART002575433-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85083651934-
dc.citation.endPage354-
dc.citation.startPage352-
dc.citation.titleJournal of Clinical Neurology-
dc.citation.volume16-
dc.citation.number2-
dc.contributor.affiliatedAuthor지민진-
dc.contributor.affiliatedAuthor정성원-
dc.contributor.affiliatedAuthor서하은-
dc.contributor.affiliatedAuthor김우람-
dc.contributor.affiliatedAuthor김소라-
dc.contributor.affiliatedAuthor이진숙-
dc.contributor.affiliatedAuthor노영-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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