Inherited epidermolysis bullosa: New diagnostics and new clinical phenotypes
Author:
Affiliation:
1. Faculty of MedicineDepartment of DermatologyMedical CenterUniversity of FreiburgUniversity of Freiburg Freiburg Germany
2. Faculty of MedicineDepartment of Human GeneticsMedical CenterUniversity of FreiburgUniversity of Freiburg Freiburg Germany
Funder
Dystrophic Epidermolysis Bullosa Research Association of America
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/exd.13668
Reference38 articles.
1. Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy
2. Molecular Heterogeneity of Blistering Disorders: The Paradigm of Epidermolysis Bullosa
3. Research Techniques Made Simple: Immunofluorescence Antigen Mapping in Epidermolysis Bullosa
4. Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification
5. EB2017—Progress in Epidermolysis Bullosa Research toward Treatment and Cure
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