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Mild phenotype of epidermolytic hyperkeratosis mimicking ichthyosis bullosa of Siemens is related to specific mutation in 2B domain of KRT1

DC Field Value Language
dc.contributor.author김송이-
dc.contributor.author김수찬-
dc.date.accessioned2014-12-18T09:14:41Z-
dc.date.available2014-12-18T09:14:41Z-
dc.date.issued2013-
dc.identifier.issn0923-1811-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/87805-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfJOURNAL OF DERMATOLOGICAL SCIENCE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdolescent-
dc.subject.MESHDNA Mutational Analysis-
dc.subject.MESHDiagnosis, Differential-
dc.subject.MESHGenetic Predisposition to Disease-
dc.subject.MESHHumans-
dc.subject.MESHHyperkeratosis, Epidermolytic/genetics*-
dc.subject.MESHHyperkeratosis, Epidermolytic/pathology-
dc.subject.MESHIchthyosis Bullosa of Siemens/diagnosis*-
dc.subject.MESHIchthyosis Bullosa of Siemens/genetics-
dc.subject.MESHIchthyosis Bullosa of Siemens/pathology-
dc.subject.MESHKeratin-1/genetics*-
dc.subject.MESHMale-
dc.subject.MESHMutation*-
dc.subject.MESHPhenotype-
dc.subject.MESHPredictive Value of Tests-
dc.subject.MESHProtein Structure, Tertiary-
dc.subject.MESHSeverity of Illness Index-
dc.subject.MESHSkin/pathology-
dc.titleMild phenotype of epidermolytic hyperkeratosis mimicking ichthyosis bullosa of Siemens is related to specific mutation in 2B domain of KRT1-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Dermatology (피부과학)-
dc.contributor.googleauthorJae Yong Sung-
dc.contributor.googleauthorSe-Woong Oh-
dc.contributor.googleauthorSong Ee Kim-
dc.contributor.googleauthorSoo-Chan Kim-
dc.identifier.doi10.1016/j.jdermsci.2013.03.001-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00627-
dc.contributor.localIdA00637-
dc.relation.journalcodeJ01370-
dc.identifier.eissn1873-569X-
dc.identifier.pmid23623204-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0923181113000686-
dc.subject.keywordEpidermolytic hyperkeratosis-
dc.subject.keywordMild phenotype-
dc.subject.keywordKeratin 1 gene-
dc.contributor.alternativeNameKim, Song Ee-
dc.contributor.alternativeNameKim, Soo Chan-
dc.contributor.affiliatedAuthorKim, Song Ee-
dc.contributor.affiliatedAuthorKim, Soo Chan-
dc.rights.accessRightsnot free-
dc.citation.volume70-
dc.citation.number3-
dc.citation.startPage220-
dc.citation.endPage222-
dc.identifier.bibliographicCitationJOURNAL OF DERMATOLOGICAL SCIENCE, Vol.70(3) : 220-222, 2013-
dc.identifier.rimsid32281-
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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