Autoimmunity and recurrent infections in partial complement C3 immunodeficiency
Author:
Publisher
Oxford University Press (OUP)
Subject
Pharmacology (medical),Rheumatology
Link
http://academic.oup.com/rheumatology/article-pdf/49/5/1017/5051067/kep444.pdf
Reference10 articles.
1. HOMOZYGOUS DEFICIENCY OF C3 IN A PATIENT WITH REPEATED INFECTIONS
2. The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency
3. Human complement component C3: cDNA coding sequence and derived primary structure.
4. Human C3 Deficiency Associated with Impairments in Dendritic Cell Differentiation, Memory B Cells, and Regulatory T Cells
5. Mixed-Pattern Immune Deposit Glomerulonephritis in a Child With Inherited Deficiency of the Third Component of Complement
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Case Report: C3 deficiency in two siblings;Frontiers in Pediatrics;2024-07-24
2. Skipping of exon 27 in C3 gene compromises TED domain and results in complete human C3 deficiency;Immunobiology;2016-05
3. Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation;BMC Nephrology;2015-03-30
4. Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe;Journal of Clinical Immunology;2015-02
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