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Two novel mutations in SASH1 identified in a familial and a sporadic generalized lentiginosis phenotype in Koreans

DC Field Value Language
dc.contributor.author이상은-
dc.date.accessioned2024-01-03T00:30:49Z-
dc.date.available2024-01-03T00:30:49Z-
dc.date.issued2023-09-
dc.identifier.issn0307-6938-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/197275-
dc.description.abstract[No abstract available]-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherBlackwell Scientific Publications-
dc.relation.isPartOfCLINICAL AND EXPERIMENTAL DERMATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHChild-
dc.subject.MESHChild, Preschool-
dc.subject.MESHEast Asian People*-
dc.subject.MESHHumans-
dc.subject.MESHLentigo* / genetics-
dc.subject.MESHMale-
dc.subject.MESHMutation-
dc.subject.MESHPhenotype-
dc.subject.MESHTumor Suppressor Proteins-
dc.titleTwo novel mutations in SASH1 identified in a familial and a sporadic generalized lentiginosis phenotype in Koreans-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Dermatology (피부과학교실)-
dc.contributor.googleauthorJae Yeon Kim-
dc.contributor.googleauthorIl Joo Kwon-
dc.contributor.googleauthorSang Eun Lee-
dc.identifier.doi10.1093/ced/llad199-
dc.contributor.localIdA02826-
dc.relation.journalcodeJ00549-
dc.identifier.eissn1365-2230-
dc.identifier.pmid37337450-
dc.identifier.urlhttps://academic.oup.com/ced/article-abstract/48/10/1171/7202413-
dc.contributor.alternativeNameLee, Sang Eun-
dc.contributor.affiliatedAuthor이상은-
dc.citation.volume48-
dc.citation.number10-
dc.citation.startPage1171-
dc.citation.endPage1173-
dc.identifier.bibliographicCitationCLINICAL AND EXPERIMENTAL DERMATOLOGY, Vol.48(10) : 1171-1173, 2023-09-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
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