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aHUS caused by complement dysregulation: new therapies on the horizon
Atypical hemolytic uremic syndrome (aHUS) is a heterogeneous disease that is caused by defective complement regulation in over 50% of cases. Mutations have been identified in genes encoding both complement regulators [complement factor H (CFH), complement factor I (CFI), complement factor H-related...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer-Verlag
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2991208/ https://ncbi.nlm.nih.gov/pubmed/20556434 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-010-1556-4 |
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