Familial C3 Glomerulopathy Associated with CFHR5 Mutations: Clinical Characteristics of 91 Patients in 16 Pedigrees

SUMMARY: BACKGROUND AND OBJECTIVES: Complement factor H and related proteins (CFHR) are key regulators of the alternative complement pathway, where loss of function mutations lead to a glomerulopathy with isolated mesangial C3 deposits without immunoglobulins. Gale et al. (12) reported on 26 patient...

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Autori principali: Athanasiou, Yiannis, Voskarides, Konstantinos, Gale, Daniel P., Damianou, Loukas, Patsias, Charalambos, Zavros, Michalis, Maxwell, Patrick H., Cook, H. Terence, Demosthenous, Panayiota, Hadjisavvas, Andreas, Kyriacou, Kyriacos, Zouvani, Ioanna, Pierides, Alkis, Deltas, Constantinos
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society of Nephrology 2011
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Original Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3109942/
https://ncbi.nlm.nih.gov/pubmed/21566112
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.09541010
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