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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Bibliografiset tiedot
Päätekijät: Feng, Shuju, Eyler, Stephen J., Zhang, Yuzhou, Maga, Tara, Nester, Carla M., Kroll, Michael H., Smith, Richard J., Afshar-Kharghan, Vahid
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society of Hematology 2013
Aiheet:
Thrombosis and Hemostasis
Linkit: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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