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A severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B.

作者信息

Bland P J, Chronnell C, Plagnol V, Kayserili H, Kelsell D P

机构信息

Centre for Cutaneous Research, The Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, U.K.

Department of Genetics, University College London, London, U.K.

出版信息

Br J Dermatol. 2015 Jul;173(1):285-7. doi: 10.1111/bjd.13627. Epub 2015 May 18.

DOI:10.1111/bjd.13627
PMID:25524567
Abstract
摘要

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