Epidermolysis bullosa - a group of skin diseases with different causes but commonalities in gene expression
Author:
Affiliation:
1. Department of Molecular Biology; University of Salzburg; Salzburg; Austria
2. Division of Molecular Dermatology and EB House Austria; Department of Dermatology; Paracelsus Medical University; Salzburg; Austria
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0625.2012.01519.x/fullpdf
Reference74 articles.
1. The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB
2. Immunohistochemical, Ultrastructural, and Molecular Features of Kindler Syndrome Distinguish It From Dystrophic Epidermolysis Bullosa
3. Overview of epidermolysis bullosa
4. The genetic basis of Weber-Cockayne epidermolysis bullosa simplex.
5. A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering
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