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Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
Epidermolysis bullosa (EB) simplex is a rare genetic condition typified by superficial bullous lesions that result from frictional trauma to the skin. Most cases are due to dominantly acting mutations in either keratin 14 (K14) or K5, the type I and II intermediate filament (IF) proteins tasked with...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2701872/ https://ncbi.nlm.nih.gov/pubmed/19587453 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI38177 |
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