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Epidermolysis Bullosa Acquitsita
EBA is a rare, acquired, chronic subepidermal bullous disease of the skin and mucosa characterized by autoantibodies to type VII collagen structures, a major component of anchoring fibrils, that attach the epidermis onto the dermis. EBA patients have tissue-bound as well as circulating anti-type VII...
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| Main Authors: | , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2012
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3234994/ https://ncbi.nlm.nih.gov/pubmed/22137228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.clindermatol.2011.03.011 |
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