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Published in 2020 at "Journal of the American Society of Nephrology : JASN"
DOI: 10.1681/asn.2019040433
Abstract: BACKGROUND Primary membranoproliferative GN, including complement 3 (C3) glomerulopathy, is a rare, untreatable kidney disease characterized by glomerular complement deposition. Complement gene mutations can cause familial C3 glomerulopathy, and studies have reported rare variants in…
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Keywords:
primary membranoproliferative;
whole genome;
complement gene;
complement ... See more keywords