CARD14 alterations in Tunisian patients with psoriasis and further characterization in European cohorts-Reference-Cited by-同舟云学术

CARD14 alterations in Tunisian patients with psoriasis and further characterization in European cohorts

Published:2015-11-17 Issue:2 Volume:174 Page:330-337
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Ammar M.¹,Jordan C.T.²,Cao L.²,Lim E.²,Bouchlaka Souissi C.¹,Jrad A.³,Omrane I.¹,Kouidhi S.¹,Zaraa I.⁴,Anbunathan H.⁵,Mokni M.⁴,Doss N.⁶,Guttman-Yassky E.⁷,El Gaaied A. B.¹,Menter A.⁸,Bowcock A.M.²⁵

Affiliation:

1. Laboratoire de Génétique d'Immunologie et de Pathologies Humaines; Faculté des Sciences de Tunis; Université Tunis El Manar; Tunis Tunisia

2. Division of Human Genetics; Department of Genetics; Washington University School of Medicine; St Louis MO 63110 U.S.A

3. Unité de Recherche de Physiologie des Agressions: Etudes Métaboliques et Endocriniennes; Faculté des Sciences de Tunis; Université Tunis El Manar; Tunis Tunisia

4. Department of Dermatology; La Rabta Hospital of Tunis; Tunis Tunisia

5. National Heart and Lung Institute; Imperial College London; London SW3 6LY U.K

6. Department of Dermatology; Military Hospital of Tunis; Tunis Tunisia

7. Department of Dermatology and the Immunology Institute; Icahn School of Medicine at the Mount Sinai Medical Center; NY U.S.A

8. Division of Dermatology; Baylor University Medical Center; Junius St, Suite 145 Dallas 3900 TX 75246 U.S.A

Funder

National Institutes of Health

University of Tunisia

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.14158/fullpdf

Reference24 articles.

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2. A classification of psoriasis vulgaris according to phenotype;Griffiths;Br J Dermatol,2007

3. Genetic epidemiology of psoriasis and psoriatic arthritis;Rahman;Ann Rheum Dis,2005

4. PSORS2 is due to mutations in CARD14;Jordan;Am J Hum Genet,2012

5. Familial pityriasis rubra pilaris is caused by mutations in CARD14;Fuchs-Telem;Am J Hum Genet,2012

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