Epidermolysis bullosa simplex due toKRT5mutations: mutation-related differences in cellular fragility and the protective effects of trimethylamineN-oxide in cultured primary keratinocytes
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2009.09615.x/fullpdf
Reference27 articles.
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2. Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility;Coulombe;J Clin Invest,2009
3. The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on Diagnosis and Classification of EB;Fine;J Am Acad Dermatol,2008
4. The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases;Szeverenyi;Hum Mutat,2008
5. A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype;Liovic;Exp Dermatol,2004
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