Novel TGM5 mutations in acral peeling skin syndrome-Reference-Cited by-同舟云学术

Novel TGM5 mutations in acral peeling skin syndrome

Published:2015-03-27 Issue:4 Volume:24 Page:285-289
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Exp Dermatol

Author:

van der Velden Jaap J. A. J.¹²,van Geel Michel¹²,Nellen Ruud G. L.¹²,Jonkman Marcel F.³,McGrath John A.⁴,Nanda Arti⁵,Sprecher Eli⁶,van Steensel Maurice A. M.¹²⁷,McLean W. H. Irwin⁸,Cassidy Andrew J.⁸

Affiliation:

1. Department of Dermatology; Maastricht University Medical Center+; Maastricht The Netherlands

2. GROW Research School for Oncology and Developmental Biology; Maastricht University Medical Center+; Maastricht The Netherlands

3. Department of Dermatology; University Medical Center Groningen; University of Groningen; Groningen The Netherlands

4. St John's Institute of Dermatology; King's College London (Guy's Campus); London UK

5. As'ad Al-Hamad Dermatology Center; Al-Sabah Hospital; Kuwait City Kuwait

6. Department of Dermatology; Tel Aviv Sourasky Medical Center; Tel Aviv Israel

7. Institute of Medical Biology; Immunos; Singapore Singapore

8. Centre for Dermatology and Genetic Medicine; Colleges of Life Sciences and Medicine, Dentistry and Nursing; Medical Sciences Institute; Dundee UK

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/exd.12650/fullpdf

Reference20 articles.

1. Peeling skin diseases: 21 cases from Turkey and a review of the literature

2. Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome

3. Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease

4. Acral peeling skin syndrome

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