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Corrigenda [Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function]

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Bibliographic Details
Main Authors: Zimmer, Andreas D. (Author) , Haußer-Siller, Ingrid (Author)
Format: Article (Journal)
Language:English
Published: 29 March 2018
In: British journal of dermatology
Year: 2018, Volume: 178, Issue: 3, Pages: 814-815
ISSN:1365-2133
DOI:10.1111/bjd.16353
Online Access:Verlag, Volltext: https://doi.org/10.1111/bjd.16353
Verlag: https://onlinelibrary.wiley.com/doi/abs/10.1111/bjd.16353
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Author Notes:Zimmer AD, Kim GJ, Hotz A, Bourrat E, Hausser I, Has C, Oji V, Stieler K, Vahlquist A, Kunde V, Weber B, Radner FPW, Leclerc-Mercier S,Schlipf N, Demmer P, Küsel J, Fischer J

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