Complementfaktor I-Mangel

Servais A et al. (2007) Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.

Vyse TJ et al. (1996) The molecular basis of hereditary complement factor I deficiency.

Sadallah S et al. (1999) Glomerulonephritis in a patient with complement factor I deficiency.

Baracho GV et al. (2003) Molecular characterization of homozygous hereditary factor I deficiency.

Alper CA et al. (1970) Studies in vivo and in vitro on an abnormality in the metabolism of C3 in a patient with increased susceptibility to infection.

Alper CA et al. (1970) Increased susceptibility to infection associated with abnormalities of complement-mediated functions and of the third component of complement (C3).

Alper CA et al. (1972) Inactivator of the third component of complement as an inhibitor in the properdin pathway.

Abramson N et al. (1971) Deficiency of C3 inactivator in man.

Thompson RA et al. (1977) A second case of human C3b inhibitor (KAF) deficiency.

OMIM.ORG article