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Uniparental disomy as a mechanism for CERS3‐mutated autosomal recessive congenital ichthyosis

Polubothu, S; Glover, M; Holder, S; Kinsler, V; (2018) Uniparental disomy as a mechanism for CERS3‐mutated autosomal recessive congenital ichthyosis. [Letter]. British Journal of Dermatology , 179 (5) pp. 1214-1215. 10.1111/bjd.16999. Green open access

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Type: Article
Title: Uniparental disomy as a mechanism for CERS3‐mutated autosomal recessive congenital ichthyosis
Open access status: An open access version is available from UCL Discovery
DOI: 10.1111/bjd.16999
Publisher version: https://doi.org/10.1111/bjd.16999
Language: English
Additional information: ©2018 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 License (https://creativecommons.org/licenses/by/4.0/).
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 > 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/10053615
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