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Items: 5

1.
Hereditary deficiency of the seventh component of complement and recurrent meningococcal infection: investigations of an Irish family using a novel haemolytic screening assay for complement activity and C7 M/N allotyping.
L. J. Egan, A. Orren, J. Doherty, R. Würzner, C. F. McCarthy
Epidemiol Infect. 1994 Oct; 113(2): 275–281. doi: 10.1017/s0950268800051700
PMCID:
PMC2271528
ArticlePDF–1.1M
2.
Combined genetic deficiency of C6 and C7 in man.
P J Lachmann, M J Hobart, P Woo
Clin Exp Immunol. 1978 Aug; 33(2): 193–203.
PMCID:
PMC1537564
ArticlePDF–2.1M
3.
Prevalence of hereditary properdin, C7 and C8 deficiencies in patients with meningococcal infections.
M Schlesinger, Z Nave, Y Levy, P E Slater, Z Fishelson
Clin Exp Immunol. 1990 Sep; 81(3): 423–427. doi: 10.1111/j.1365-2249.1990.tb05350.x
PMCID:
PMC1534994
ArticlePDF–923K
4.
Hereditary C7 deficiency. Diagnosis and HLA studies in a French-Canadian family.
J M Delâge, P Bergeron, J Simard, G Lehner-Netsch, E Prochazka
J Clin Invest. 1977 Nov; 60(5): 1061–1069. doi: 10.1172/JCI108857
PMCID:
PMC372458
ArticlePDF–1.3M
5.
Hereditary deficiency of the seventh component of complement.
J T Boyer, E P Gall, M E Norman, U R Nilsson, T S Zimmerman
J Clin Invest. 1975 Oct; 56(4): 905–913. doi: 10.1172/JCI108170
PMCID:
PMC301946
ArticlePDF–1.5M

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