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Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome
Complement dysregulation leads to atypical hemolytic uremic syndrome (aHUS), while ADAMTS13 deficiency causes thrombotic thrombocytopenic purpura. We investigated whether genetic variations in the ADAMTS13 gene partially explain the reduced activity known to occur in some patients with aHUS. We meas...
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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 of Hematology
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3750341/ https://ncbi.nlm.nih.gov/pubmed/23847193 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-03-492421 |
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