Publication:
Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement

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dc.contributor.authorELÇİOĞLU, HURİYE NURSEL
dc.contributor.authorsMansur, A. Tuelin; Elcioglu, Nursel H.; Aydingoz, Ikbal E.; Akkaya, A. Deniz; Serdar, Zehra Asiran; Herz, Corinna; Bruckner-Tuderman, Leena; Has, Cristina
dc.date.accessioned2022-03-11T23:50:40Z
dc.date.accessioned2026-01-11T13:46:25Z
dc.date.available2022-03-11T23:50:40Z
dc.date.issued2007
dc.identifier.doi10.2340/00015555-0314
dc.identifier.issn0001-5555
dc.identifier.pubmed17989907
dc.identifier.urihttps://hdl.handle.net/11424/223127
dc.identifier.wosWOS:000251213300025
dc.language.isoeng
dc.publisherACTA DERMATO-VENEREOLOGICA
dc.relation.ispartofACTA DERMATO-VENEREOLOGICA
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectSKIN FRAGILITY
dc.subjectPROTEIN
dc.subjectGENE
dc.subjectKINDLIN-1
dc.subjectNONSENSE
dc.titleNovel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement
dc.typeother
dc.type.subletter
dspace.entity.typePublication
oaire.citation.endPage565
oaire.citation.issue6
oaire.citation.startPage563
oaire.citation.titleACTA DERMATO-VENEREOLOGICA
oaire.citation.volume87

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