In Search of C3G Tissue Biomarkers

Volume: 4, Issue: 10, Pages: 1359 - 1361
Published: Oct 1, 2019
Abstract
See Clinical Research on Page 1387 See Clinical Research on Page 1387 Complement (C) 3 glomerulopathy (C3G) is a rare, complement-mediated disorder that encompasses C3 glomerulonephritis (C3GN) and dense deposit disease (DDD). Drivers can be acquired autoantibodies and/or genetic mutations in distinct components and regulatory factors of the complement alternative pathway (CAP; Figure 1). Most common are autoantibodies, such as the C3 nephritic...
Paper Details
Title
In Search of C3G Tissue Biomarkers
Published Date
Oct 1, 2019
Volume
4
Issue
10
Pages
1359 - 1361
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