Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences inFLGmutations between European and Asian populations
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2009.09112.x/fullpdf
Reference12 articles.
1. Ichthyosis vulgaris: identification of a defect in synthesis of filaggrin correlated with an absence of keratohyaline granules;Sybert;J Invest Dermatol,1985
2. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris;Smith;Nat Genet,2006
3. An update on molecular aspects of the non-syndromic ichthyoses;Akiyama;Exp Dermatol,2008
4. Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema;Sandilands;Nat Genet,2007
5. Filaggrin in atopic dermatitis;O’Regan;J Allergy Clin Immunol,2008
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