Volume 173, Issue 1 pp. 285-287
Research Letter

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

P.J. Bland

P.J. Bland

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

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C. Chronnell

C. Chronnell

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

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V. Plagnol

V. Plagnol

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

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H. Kayserili

H. Kayserili

Medical Genetics Department, Istanbul Medical Faculty, Istanbul University, Millet cad, 34093 Fatih Istanbul, Turkey

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D.P. Kelsell

Corresponding Author

D.P. Kelsell

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

Correspondence: David P. Kelsell.

E-mail: [email protected]

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First published: 18 December 2014
Citations: 1
Funding sources: This work was supported by funding from the Samuel Hardgrave Harlequin Ichthyosis Research Trust (SHHiRT) and the Ichthyosis Support Group (ISG) awarded to D.P.K.
Conflicts of interest: none declared.
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