Acral peeling skin syndrome associated with a novelCSTAgene mutation-Reference-Cited by-同舟云学术

Acral peeling skin syndrome associated with a novelCSTAgene mutation

Published:2015-12-18 Issue:4 Volume:41 Page:394-398
ISSN:0307-6938
Container-title:Clinical and Experimental Dermatology
language:en
Short-container-title:Clin Exp Dermatol

Author:

Muttardi K.¹,Nitoiu D.²,Kelsell D. P.²,O'Toole E. A.²,Batta K.¹

Affiliation:

1. Department of Dermatology; Watford General Hospital; Watford Hertfordshire UK

2. Centre for Cell Biology and Cutaneous Research; Blizard Institute; Barts and the London School of Medicine and Dentistry; Queen Mary University of London; London UK

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ced.12777/fullpdf

Reference9 articles.

1. Acral peeling skin syndrome: a clinically and genetically heterogeneous disorder;Pavlovic;Pediatr Dermatol,2012

2. Mutations in CSTA, encoding cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion;Blaydon;Am J Hum Genet,2011

3. Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A;Krunic;Pediatr Dermatol,2013

4. Association analysis of the skin barrier gene cystatin A at the PSORS5 locus in psoriatic patients: evidence for interaction between PSORS1 and PSORS5;Vasilopoulos;Eur J Hm Genet,2008

5. Cystatin A inhibits IL-8 production by keratinocytes stimulated with Der p 1 and Der f 1: Biochemical skin barrier against mite cysteine proteases;Kato;J Allergy Clin Immunol,2005

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