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Hans E. Nielsen, Claus Koch, Pascal Magnussen & Inga Lind. (1989) Complement Deficiencies in Selected Groups of Patients with Meningococcal Disease. Scandinavian Journal of Infectious Diseases 21:4, pages 389-396.
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Lone Schejbel, Dag Fadnes, Henrik Permin, Knut Tore Lappegård, Peter Garred & Tom Eirik Mollnes. (2013) Primary complement C5 deficiencies – Molecular characterization and clinical review of two families. Immunobiology 218:10, pages 1304-1310.
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P. Aguilar-Ramirez, E.S. Reis, M.P.C. Florido, A.S. Barbosa, C.S. Farah, B.T. Costa-Carvalho & L. Isaac. (2009) Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability. Molecular Immunology 46:10, pages 2116-2123.
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Eva Delgado-Cerviño, Gumersindo Fontán & Margarita López-Trascasa. (2005) C5 complement deficiency in a Spanish family. Molecular Immunology 42:1, pages 105-111.
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Ö. Sanal, M. Loos, F. Ersoy, G. Kanra, G. Seçmeer & I. Tezcan. (1992) Complement component deficiencies and infection: C5, C8 and C3 deficiencies in three families. European Journal of Pediatrics 151:9, pages 676-679.
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HANS ERIK NIELSEN, SEVERIN OLESEN LARSEN & THORA VIKINGSDOTTIR. (1992) Rate-limiting components and reaction steps in complement-mediated haemolysis. APMIS 100:7-12, pages 1053-1060.
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J E FigueroaP Densen. (1991) Infectious diseases associated with complement deficiencies. Clinical Microbiology Reviews 4:3, pages 359-395.
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A. Gianella-Borradori, L. Borradori, P.M. Schneider, E. Gautier & P.J. Späth. (1990) Combined complete C5 and partial C4 deficiency in humans: Clinical consequences and complement-mediated functions in vitro. Clinical Immunology and Immunopathology 55:1, pages 41-55.
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