Netherton syndrome resulting from a novel homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigree

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dc.contributor.authorLai-Cheong, J.
dc.contributor.authorFong, K.
dc.contributor.authorAkdeniz, S.
dc.contributor.authorIsi, H.
dc.contributor.authorTaskesen, M.
dc.contributor.authorMcGrath, J. A.
dc.date.accessioned2024-04-24T17:47:42Z
dc.date.available2024-04-24T17:47:42Z
dc.date.issued2011
dc.departmentDicle Üniversitesien_US
dc.description91st Annual Meeting of the British-Association-of-the-Dermatologists -- JUL 05-07, 2011 -- London, ENGLANDen_US
dc.description.abstract[Abstract Not Available]en_US
dc.description.sponsorshipBritish Assoc Dermatolen_US
dc.identifier.endpage118en_US
dc.identifier.issn0007-0963
dc.identifier.startpage118en_US
dc.identifier.urihttps://hdl.handle.net/11468/22699
dc.identifier.volume165en_US
dc.identifier.wosWOS:000292456000246
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.relation.ispartofBritish Journal of Dermatologyen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keyword]en_US
dc.titleNetherton syndrome resulting from a novel homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigreeen_US
dc.typeConference Objecten_US

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