Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome

The pathogenesis of atypical hemolytic uremic syndrome (aHUS) is strongly linked to dysregulation of the alternative pathway of the complement system. Mutations in complement genes have been identified in about two-thirds of cases, with 5% to 15% being in C3. In this study, 23 aHUS-associated geneti...

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Bibliografische gegevens
Gepubliceerd in:Blood
Hoofdauteurs: Schramm, Elizabeth C., Roumenina, Lubka T., Rybkine, Tania, Chauvet, Sophie, Vieira-Martins, Paula, Hue, Christophe, Maga, Tara, Valoti, Elisabetta, Wilson, Valerie, Jokiranta, Sakari, Smith, Richard J. H., Noris, Marina, Goodship, Tim, Atkinson, John P., Fremeaux-Bacchi, Veronique
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society of Hematology 2015
Onderwerpen:
Immunobiology
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4392009/
https://ncbi.nlm.nih.gov/pubmed/25608561
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2014-10-609073
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