Multiple facets of desmoglein 1 mutations
Author:
Affiliation:
1. Department of Dermatology; Medical Center - University of Freiburg; Faculty of Medicine; Hauptstrasse 7 79104 Freiburg Germany
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.16937/fullpdf
Reference9 articles.
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2. Hereditary palmoplantar keratodermas. Part I. Non-syndromic palmoplantar keratodermas: classification, clinical and genetic features;Guerra;J Eur Acad Dermatol Venereol,2018
3. Striate palmoplantar keratoderma resulting from a missense mutation in DSG1;Vodo;Br J Dermatol,2018
4. Desmoglein 1-dependent suppression of EGFR signaling promotes epidermal differentiation and morphogenesis;Getsios;J Cell Biol,2009
5. SAM syndrome is characterized by extensive phenotypic heterogeneity;Taiber;Exp Dermatol,2018
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