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Known mutations/causes associated with C3GN
| Autoantibodies to C3 convertase |
| Autoantibodies to factor H |
| Autoantibodies to factor B |
| Properdin deficiency |
| C3 nephretic factor |
| Complement factor H mutation screening identified the H402 allele and V62 allele |
| Heterozygous mutations in factor I gene |
| Heterozygous mutation in CD 46 gene (membrane cofactor protein) |
| Mutation in the gene for complement factor H-related protein 5 |
