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dc.contributor.author허정원*
dc.contributor.author문영철*
dc.contributor.author정태동*
dc.contributor.author박설희*
dc.date.accessioned2021-01-20T16:30:03Z-
dc.date.available2021-01-20T16:30:03Z-
dc.date.issued2019*
dc.identifier.issn2059-2302*
dc.identifier.issn2059-2310*
dc.identifier.otherOAK-24615*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/256015-
dc.description.abstractLoss or decrease in expression of human HLA caused by somatic mutations of HLA genes has been reported in various malignancies. However, mutations in the HLA-DR gene have been rarely noted in hematologic malignancies. Here, we report a case of myelodysplastic syndrome (MDS) with a novel point mutation in exon 2 of the HLA-DRBI*04:03 gene pertaining to a silent mutation (c.357A > T [ p.Thr=]). When compared before and after anticancer drug treatment and to the results from the full HLA-matching sibling donor, mutation of the HLA-DRB 1 gene suggests clonal evolution. In conclusion, we report a new DRBI*04:03 mutation in an MDS patient at diagnosis that results in a synonymous substitution with unknown clinical impact.*
dc.languageEnglish*
dc.publisherWILEY*
dc.subjectHLA-DR gene*
dc.subjectmutation*
dc.subjectmyelodysplastic syndrome*
dc.titleSomatic mutation of HLA-DRB1*04:03 in a patient with myelodysplastic syndrome at diagnosis*
dc.typeArticle*
dc.relation.issue4*
dc.relation.volume93*
dc.relation.indexSCOPUS*
dc.relation.startpage216*
dc.relation.lastpage219*
dc.relation.journaltitleHLA*
dc.identifier.doi10.1111/tan.13490*
dc.identifier.wosidWOS:000462353100004*
dc.identifier.scopusid2-s2.0-85063008498*
dc.author.googlePark, Sholhui*
dc.author.googleJeong, Tae D.*
dc.author.googleMun, Yeung C.*
dc.author.googleSeo, Dongchun*
dc.author.googleIm, Jisu*
dc.author.googleHuh, Jungwon*
dc.contributor.scopusid허정원(7102258576)*
dc.contributor.scopusid문영철(7003363716)*
dc.contributor.scopusid정태동(54401279700)*
dc.contributor.scopusid박설희(56529819400)*
dc.date.modifydate20260901081000*
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의과대학 > 의학과 > Journal papers
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