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Kim, Jin Soo
유전체 교정 연구단
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Base Editing in Progeria

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dc.contributor.authorJin‑Soo Kim-
dc.contributor.authorEriksson, Maria-
dc.date.accessioned2021-07-05T02:30:15Z-
dc.date.accessioned2021-07-05T02:30:15Z-
dc.date.available2021-07-05T02:30:15Z-
dc.date.available2021-07-05T02:30:15Z-
dc.date.created2021-04-21-
dc.date.issued2021-04-
dc.identifier.issn0028-4793-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/9839-
dc.description.abstractThe Hutchinson?Gilford progeria syndrome is an autosomal dominant disease caused by a single point mutation in LMNA, which encodes the lamin A and C proteins. Recent experiments have shown that life span in a mouse model of the disease was extended through DNA base editing.-
dc.language영어-
dc.publisherMASSACHUSETTS MEDICAL SOC-
dc.titleBase Editing in Progeria-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000637799800016-
dc.identifier.scopusid2-s2.0-85103876458-
dc.identifier.rimsid75407-
dc.contributor.affiliatedAuthorJin‑Soo Kim-
dc.identifier.doi10.1056/NEJMcibr2100661-
dc.identifier.bibliographicCitationNEW ENGLAND JOURNAL OF MEDICINE, v.384, no.14, pp.1364 - 1366-
dc.relation.isPartOfNEW ENGLAND JOURNAL OF MEDICINE-
dc.citation.titleNEW ENGLAND JOURNAL OF MEDICINE-
dc.citation.volume384-
dc.citation.number14-
dc.citation.startPage1364-
dc.citation.endPage1366-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
Appears in Collections:
Center for Genome Engineering(유전체 교정 연구단) > 1. Journal Papers (저널논문)
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