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A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma

Kinsler, VA; Drury, S; Khan, A; Waelchli, R; Rukaite, G; Barnicoat, A; Lench, N; ... O'Shaughnessy, RF; + view all (2015) A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma. Br J Dermatol , 172 (1) 262 - 264. 10.1111/bjd.13361. Green open access

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Type: Article
Title: A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1111/bjd.13361
Publisher version: http://dx.doi.org/10.1111/bjd.13361
Language: English
Additional information: © 2014 The Authors. British Journal of Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Genetics and Genomic Medicine Dept
URI: https://discovery.ucl.ac.uk/id/eprint/1443381
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