A Novel Homozygous Nonsense Mutation in The Calpastatin (CAST) Gene Associated with Peeling Skin Phenotype in A Child

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dc.contributor.authorSaricaoglu, Hayriye
dc.contributor.authorTemel, Sehime
dc.contributor.authorZorlu, Ozge
dc.contributor.authorTurkgenc, Burcu
dc.contributor.authorKutuk, Ozgur
dc.contributor.authorKarakas, Bahriye
dc.contributor.authorKiran, Ummuhan
dc.contributor.authorErguner, Bekir
dc.contributor.authorYakicier, Cengiz
dc.contributor.orcIDhttps://orcid.org/0000-0001-9854-7220en_US
dc.contributor.researcherIDAAH-1671-2019en_US
dc.date.accessioned2023-05-11T06:44:51Z
dc.date.available2023-05-11T06:44:51Z
dc.date.issued2018
dc.identifier.endpageAB16en_US
dc.identifier.issn0190-9622en_US
dc.identifier.issue3en_US
dc.identifier.startpageAB16en_US
dc.identifier.urihttp://hdl.handle.net/11727/8963
dc.identifier.volume79en_US
dc.identifier.wos000440565900063en_US
dc.language.isoengen_US
dc.relation.journalJOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGYen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleA Novel Homozygous Nonsense Mutation in The Calpastatin (CAST) Gene Associated with Peeling Skin Phenotype in A Childen_US
dc.typeConference Objecten_US

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