CFHR gene variations provide insights in the pathogenesis of the kidney diseases atypical hemolytic uremic syndrome and C3 glomerulopathy.

Zipfel PF, Wiech T, Stea ED, Skerka C (2020) CFHR gene variations provide insights in the pathogenesis of the kidney diseases atypical hemolytic uremic syndrome and C3 glomerulopathy. J Am Soc Nephrol 31(2), 241-256. (Review)

Leibniz-HKI-Autor*innen

Christine Skerka
Peter F. Zipfel

Identifier

doi: 10.1681/ASN.2019050515

PMID: 31980588