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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Med Genet
Päätekijät: Feitz, Wouter J. C., van de Kar, Nicole C. A. J., Orth-Höller, Dorothea, van den Heuvel, Lambert P. J. W., Licht, Christoph
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer Medizin 2018
Aiheet:
Linkit: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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