Associated Papers
Defective C3d caused by C3 p.W1034R in inherited atypical hemolytic uremic syndrome.
Tsuchida M et al.
Molecular Genetics & Genomic Medicine, 2024
Genotype-phenotype correlations of low-frequency variants in the complement system in renal disease and age-related macular degeneration.
Geerlings MJ et al.
Clinical Genetics, 2018
29888403 (PubMed )
Supplement: CGE-94-330-s001.zip › Appendix_S1 › Table_S4.xlsx › C3
Regulators of complement activity mediate inhibitory mechanisms through a common C3b-binding mode.
Forneris F et al.
The Embo Journal, 2016
27013439 (PubMed )
Supplement: EMBJ-35-1133-s001.pdf
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