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Defining keratin protein function in skin epithelia: Epidermolysis Bullosa Simplex and its aftermath
Epidermolysis bullosa simplex (EBS) is a rare genetic condition typified by superficial bullous lesions following incident frictional trauma to the skin. Most cases of EBS are due to dominantly-acting mutations in keratin 14 (K14) or K5, the type I and II intermediate filament (IF) proteins that co-...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279600/ https://www.ncbi.nlm.nih.gov/pubmed/22277943 http://dx.doi.org/10.1038/jid.2011.450 |