(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)
Beteiligte Forschungseinheiten
Identifier
doi: 10.1681/ASN.2019050515
PMID: 31980588