Genetic analysis of the complement pathway in C3 glomerulopathy
Author:
Affiliation:
1. National Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China
2. Division of Nephrology, Jinling Hospital, Southern Medical University, Nanjing, China
Funder
National Natural Science Foundation of China
Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Link
http://academic.oup.com/ndt/article-pdf/33/11/1919/26182581/gfy033.pdf
Reference28 articles.
1. C3 glomerulopathy: consensus report;Pickering;Kidney Int,2013
2. Membranoproliferative glomerulonephritis: pathogenetic heterogeneity and proposal for a new classification;Sethi;Semin Nephrol,2011
3. C3 glomerulopathy: a new classification;Fakhouri;Nat Rev Nephrol,2010
4. Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a ‘Kidney Disease: Improving Global Outcomes’ (KDIGO) Controversies Conference;Goodship;Kidney Int,2017
5. Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome;Servais;J Med Genet,2007
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