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Hereditary platelet function disorder from RASGRP2 gene mutations encoding CalDAG-GEFI identified by whole-exome sequencing in a Korean woman with severe bleeding

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dc.contributor.authorYun, Jae Won-
dc.contributor.authorLee, Ki-O-
dc.contributor.authorJung, Chul Won-
dc.contributor.authorOh, Soo-Young-
dc.contributor.authorKim, Sun-Hee-
dc.contributor.authorChoi, Chul Won-
dc.contributor.authorKim, Hee-Jin-
dc.date.accessioned2021-09-01T14:47:03Z-
dc.date.available2021-09-01T14:47:03Z-
dc.date.created2021-06-18-
dc.date.issued2019-05-31-
dc.identifier.issn0390-6078-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/65356-
dc.languageEnglish-
dc.language.isoen-
dc.publisherFERRATA STORTI FOUNDATION-
dc.subjectDYSFUNCTION-
dc.subjectDIAGNOSIS-
dc.subjectVARIANTS-
dc.titleHereditary platelet function disorder from RASGRP2 gene mutations encoding CalDAG-GEFI identified by whole-exome sequencing in a Korean woman with severe bleeding-
dc.typeArticle-
dc.contributor.affiliatedAuthorChoi, Chul Won-
dc.identifier.doi10.3324/haematol.2019.218487-
dc.identifier.scopusid2-s2.0-85066936772-
dc.identifier.wosid000469839300012-
dc.identifier.bibliographicCitationHAEMATOLOGICA, v.104, no.6, pp.E274 - E276-
dc.relation.isPartOfHAEMATOLOGICA-
dc.citation.titleHAEMATOLOGICA-
dc.citation.volume104-
dc.citation.number6-
dc.citation.startPageE274-
dc.citation.endPageE276-
dc.type.rimsART-
dc.type.docTypeEditorial Material-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaHematology-
dc.relation.journalWebOfScienceCategoryHematology-
dc.subject.keywordPlusDYSFUNCTION-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusVARIANTS-
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