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The genetics of atypical hemolytic uremic syndrome
Atypical hemolytic uremic syndrome (aHUS) is a disorder characterized by thrombocytopenia and microangiopathic hemolytic anemia due to endothelial injury. aHUS is felt to be caused by defective complement regulation due to underlying genetic mutations in complement regulators or activators, most oft...
保存先:
| 出版年: | Med Genet |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer Medizin
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6404389/ https://ncbi.nlm.nih.gov/pubmed/30930551 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11825-018-0216-0 |
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