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- W4301595390 abstract "C3 is a crucial protein of the complement system. Congenital C3 deficiency is extremely rare and manifests through recurrent, severe infections and should always be considered as a differential diagnosis of recurrent pyogenic infections. We report a case of a patient with a novel C3 gene mutation, responsible for complete C3 deficiency with impaired complement system activation and recurrent infections." @default.
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- W4301595390 date "2022-10-05" @default.
- W4301595390 modified "2023-09-26" @default.
- W4301595390 title "Recurrent pyogenic infections caused by a novel Gln1420* mutation in the C3 gene" @default.
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- W4301595390 doi "https://doi.org/10.3389/fped.2022.1017195" @default.
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