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IgA nephropathy in patients with congenital C9 deficiency

✍ Scribed by Yoshioka, Kazuo; Takemura, Tsukasa; Akano, Norihisa; Okada, Mitsuru; Yagi, Kazuro; Maki, Sunao; Inai, Shinya; Akita, Hironobu; Koitabashi, Yasushi; Takekoshi, Yasuo

Book ID
109882237
Publisher
Nature Publishing Group
Year
1992
Tongue
English
Weight
825 KB
Volume
42
Category
Article
ISSN
0085-2538

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IgA nephropathy (IgAN) is the most common form of chronic glomerulonephritis. Although glomerular deposition of complement components is well known, the evidence of serological complement activation in IgAN is inconclusive. We hypothesized that serum levels of complement components and regulatory pr