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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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| Autori principali: | , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society of Hematology
2013
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| Soggetti: | |
| Accesso online: | 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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