Abstract
Clinical and Experimental DermatologyVolume 36, Issue 7 p. 831-831 Free Access Erratum This article corrects the following: New homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigree with Netherton syndrome K. Fong, S. Akdeniz, H. Isi, M. Taskesen, J. A. McGrath, J. E. Lai-Cheong, Volume 36Issue 4Clinical and Experimental Dermatology pages: 412-415 First Published online: December 24, 2010 First published: 20 September 2011 https://doi.org/10.1111/j.1365-2230.2011.04193.xAboutSectionsPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat In the article by Fong et al.1 there was an error in the author affiliations. The corrected list of affiliations appears below: K. Fong, S. Akdeniz,* H. Isi,* M. Taskesen,* J. A. McGrath and J. E. Lai-Cheon Genetic Skin Disease Group, St John’s Institute of Dermatology, King’s College London (Guy’s Campus), London, UK; and *Department of Dermatology, Genetics and Pediatrics, Dicle Medical University, Diyarbakir, Turkey. We apologize for this error. Reference 1 Fong K, Akdeniz S, Isi H et al. New homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigree with Netherton syndrome. Clin Exp Dermatol 2011; 36: 412– 5. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Volume36, Issue7October 2011Pages 831-831 ReferencesRelatedInformation
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