Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2009.03469.x/fullpdf
Reference20 articles.
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2. The prevalence of childhood atopic eczema in a general population;Kay;J Am Acad Dermatol,1994
3. Prevalence of atopic eczema in the community: the Lothian Atopic Dermatitis study;Herd;Br J Dermatol,1996
4. The occurrence of atopic dermatitis in north Europe: an international questionnaire study;Schultz-Larsen;J Am Acad Dermatol,1996
5. Is the prevalence of atopic dermatitis increasing?;Williams;Clin Exp Dermatol,1992
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1. Increased loss‐of‐function filaggrin gene mutation prevalence in atopic dermatitis patients across northern latitudes indicates genetic fitness: A systematic review and meta‐analysis;Experimental Dermatology;2024-07
2. Association between polymorphisms and atopic dermatitis susceptibility: A systematic review and meta-analysis;Gene;2024-06
3. Mutacii 2282del4, R501X, R2447X, S3247X fillagrina pri atopicheskom dermatite;Вестник Российского государственного медицинского университета;2024-02
4. Filaggrin loss-of-function mutations 2282del4, R501X, R2447X and S3247X in atopic dermatitis;Bulletin of Russian State Medical University;2024-02
5. Inflammation-related proteins in blood after dermal exposure to some common chemicals depend on the skin barrier gene filaggrin - a human experimental study;Environmental Toxicology and Pharmacology;2024-01
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