Filaggrin loss-of-function variant contributes to atopic dermatitis risk in the population of Northern Germany-Reference-Cited by-同舟云学术

Filaggrin loss-of-function variant contributes to atopic dermatitis risk in the population of Northern Germany

Published:2006-08-23 Issue:5 Volume:155 Page:1093-1094
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:

Author:

Ruether A.,Stoll M.,Schwarz T.,Schreiber S.,Fölster-Holst R.

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2006.07500.x/fullpdf

Reference11 articles.

1. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris;Smith;Nat Genet,2006

2. Filaggrin: a keratin filament associated protein;Dale;Ann NY Acad Sci,1985

3. Ichthyosis vulgaris. A clinical and histopathological study of patients and their close relatives in the autosomal dominant and sex-linked forms of the disease;Kuokkanen;Acta Derm Venereol (Stockh),1969

4. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis;Palmer;Nat Genet,2006

5. Lack of association of SPINK5 polymorphisms with nonsyndromic atopic dermatitis in the population of Northern Germany;Fölster-Holst;Br J Dermatol,2005

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