Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis-Reference-Cited by-同舟云学术

Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis

Published:2006-08 Issue:8 Volume:126 Page:1770-1775
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Sandilands Aileen,O'Regan Gráinne M.,Liao Haihui,Zhao Yiwei,Terron-Kwiatkowski Ana,Watson Rosemarie M.,Cassidy Andrew J.,Goudie David R.,Smith Frances J.D.,Irwin McLean W.H.,Irvine Alan D.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference23 articles.

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3. A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome;Cassidy;Am J Hum Genet,2005

4. Mapping of the associated phenotype of an absent granular layer in ichthyosis vulgaris to the epidermal differentiation complex on chromosome 1;Compton;Exp Dermatol,2002

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

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