Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS

Atypical hemolytic uremic syndrome (aHUS) is a rare disease characterized by microangiopathic hemolytic anemia, thrombocytopenia and renal failure. It is caused by genetic or acquired defects of the complement alternative pathway. Factor H autoantibodies (anti-FHs) have been reported in 10% of aHUS...

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Detaylı Bibliyografya
Yayımlandı:Front Immunol
Asıl Yazarlar: Valoti, Elisabetta, Alberti, Marta, Iatropoulos, Paraskevas, Piras, Rossella, Mele, Caterina, Breno, Matteo, Cremaschi, Alessandra, Bresin, Elena, Donadelli, Roberta, Alizzi, Silvia, Amoroso, Antonio, Benigni, Ariela, Remuzzi, Giuseppe, Noris, Marina
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2019
Konular:
Immunology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6504697/
https://ncbi.nlm.nih.gov/pubmed/31118930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2019.00853
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