Complement phenotypes in glomerulonephritis: Increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura-Reference-Cited by-同舟云学术

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Complement phenotypes in glomerulonephritis: Increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura

Published:1984-12 Issue:6 Volume:26 Page:855-860
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

McLean Robert H.,Wyatt Robert J.,Julian Bruce A.

Publisher

Elsevier BV

Subject

Nephrology

Reference42 articles.

1. The genetics of the complement system;Lachmann,1979

2. Genetic polymorphism of human complement proteins;Hauptmann;Rev Fr Transfus Immunohematol,1979

3. Genetic polymorphism of human C4–binding protein;Rodríguez de Córdoba;J Immunol,1983

4. Genetic polymorphism of human factor H (B H);Rodríguez de Córdoba;J Immunol,1984

5. Structural polymorphism of the fourth component of human complement;Rosenfield;J Clin Invest,1969

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1. Complement or insult: the emerging link between complement cascade deficiencies and pathology of myeloid malignancies;Journal of Leukocyte Biology;2024-06-05

2. IgA vasculitis update: Epidemiology, pathogenesis, and biomarkers;Frontiers in Immunology;2022-10-03

3. Complement C4, Infections, and Autoimmune Diseases;Frontiers in Immunology;2021-07-14

4. Clinical characteristics of IgA nephropathy associated with low complement 4 levels;Renal Failure;2014-12-24

5. C4 Deficiency Is a Predisposing Factor for Streptococcus pneumoniae–Induced Autoantibody Production;The Journal of Immunology;2014-10-22

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