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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Gepubliceerd in:Front Immunol
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Frontiers Media S.A. 2019
Onderwerpen:
Immunology
Online toegang: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
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items