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Minor Role of Plasminogen in Complement Activation on Cell Surfaces
Atypical hemolytic uremic syndrome (aHUS) is a rare, but severe thrombotic microangiopathy. In roughly two thirds of the patients, mutations in complement genes lead to uncontrolled activation of the complement system against self cells. Recently, aHUS patients were described with deficiency of the...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Public Library of Science
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670116/ https://www.ncbi.nlm.nih.gov/pubmed/26637181 http://dx.doi.org/10.1371/journal.pone.0143707 |