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A Case of HSP Carrying c.1537-11A > G Mutation of the SPAST Gene Presented as Stiff-Person Syndrome

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dc.contributor.authorBae, J.-H.-
dc.contributor.authorJeong, H.-B.-
dc.contributor.authorKim, H.-
dc.contributor.authorSong, K.-S.-
dc.contributor.authorPark, S.-T.-
dc.contributor.authorAhn, S.-W.-
dc.date.accessioned2021-11-10T00:40:29Z-
dc.date.available2021-11-10T00:40:29Z-
dc.date.issued2021-07-
dc.identifier.issn0028-3886-
dc.identifier.issn1998-4022-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/51252-
dc.description.abstract[No abstract available]-
dc.format.extent2-
dc.language영어-
dc.language.isoENG-
dc.publisherWolters Kluwer Medknow Publications-
dc.titleA Case of HSP Carrying c.1537-11A > G Mutation of the SPAST Gene Presented as Stiff-Person Syndrome-
dc.typeArticle-
dc.identifier.doi10.4103/0028-3886.325344-
dc.identifier.bibliographicCitationNeurology India, v.69, no.4, pp 1053 - 1054-
dc.description.isOpenAccessN-
dc.identifier.wosid000755032000058-
dc.identifier.scopusid2-s2.0-85115072239-
dc.citation.endPage1054-
dc.citation.number4-
dc.citation.startPage1053-
dc.citation.titleNeurology India-
dc.citation.volume69-
dc.identifier.urlhttps://journals.lww.com/neur/fulltext/2021/69040/a_case_of_hsp_carrying_c_1537_11a___g_mutation_of.58.aspx-
dc.type.docTypeLetter-
dc.publisher.location인도-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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