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Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome

DC Field Value Language
dc.contributor.author김송이-
dc.contributor.author김수찬-
dc.contributor.author이상은-
dc.date.accessioned2017-10-26T07:12:05Z-
dc.date.available2017-10-26T07:12:05Z-
dc.date.issued2016-
dc.identifier.issn1013-9087-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/151730-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.publisherKorean Dermatological Association-
dc.relation.isPartOfANNALS OF DERMATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleHomozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome-
dc.typeArticle-
dc.publisher.locationKorea-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentYonsei Biomedical Research Center-
dc.contributor.googleauthorSeung Joon Oh-
dc.contributor.googleauthorSong-Ee Kim-
dc.contributor.googleauthorSang Eun Lee-
dc.contributor.googleauthorSoo-Chan Kim-
dc.identifier.doi10.5021/ad.2016.28.4.503-
dc.contributor.localIdA00637-
dc.contributor.localIdA02826-
dc.contributor.localIdA00627-
dc.relation.journalcodeJ00158-
dc.identifier.eissn2005-3894-
dc.relation.journalsince1989~-
dc.identifier.pmid27489438-
dc.contributor.alternativeNameKim, Song Ee-
dc.contributor.alternativeNameKim, Soo Chan-
dc.contributor.alternativeNameLee, Sang Eun-
dc.contributor.affiliatedAuthorKim, Soo Chan-
dc.contributor.affiliatedAuthorLee, Sang Eun-
dc.contributor.affiliatedAuthorKim, Song Ee-
dc.citation.volume28-
dc.citation.number4-
dc.citation.startPage503-
dc.citation.endPage505-
dc.identifier.bibliographicCitationANNALS OF DERMATOLOGY, Vol.28(4) : 503-505, 2016-
dc.date.modified2017-10-24-
dc.identifier.rimsid45743-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
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