Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profile
Author:
Affiliation:
1. Department of Dermatology; University of Münster; Münster Germany
2. Institute of Biostatistics and Clinical Research; University of Münster; Münster Germany
3. Department of Dermatology; University of Heidelberg; Heidelberg Germany
Funder
German Federal Ministry for Education and Research
Medical Faculty
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jdv.12079/fullpdf
Reference32 articles.
1. Autosomal Dominant Ichthyosis Vulgaris
2. Clinical features of autosomal dominant and sex-linked ichthyosis in an English population;Wells;Br Med J,1966
3. Ichthyosis: clinical manifestations and practical treatment options;Oji;Am J Clin Dermatol,2009
4. Filaggrin null mutations and childhood atopic eczema: a population-based case-control study;Brown;J Allergy Clin Immunol,2008
5. FLG mutations in ichthyosis vulgaris and atopic eczema: spectrum of mutations and population genetics;Akiyama;Br J Dermatol,2010
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