A novel mutation in a patient with a deficiency of the eighth component of complement associated with recurrent meningococcal meningitis.
Arnold DF, Roberts AG, Thomas A, Ferry B, Morgan BP, Chapel H J Clin Immunol 2009(5): 691-5
[PubMed abstract].
1997
Molecular, genetic, and functional analysis of homozygous C8 beta-chain deficiency in two siblings.
Kotnik V, Luznik-Bufon T, Schneider PM, Kirschfink M Immunopharmacology 1997(1-2): 215-21
[PubMed abstract].
1995
Delineation of additional genetic bases for C8 beta deficiency. Prevalence of null alleles and predominance of C-->T transition in their genesis.
Saucedo L, Ackermann L, Platonov AE, Gewurz A, Rakita RM, Densen P J Immunol 1995(10): 5022-8
[PubMed abstract].
1994
Polymorphism of the complement C8A and -B genes in two families with C8 beta deficiency and neisserial infections.
Barba GM, Kaufmann TJ, Schneider PM, Rittner C, Brai M Clin Immunol Immunopathol 1994(1): 83-9
[PubMed abstract].
1993
Meningococcal disease in patients with late complement component deficiency: studies in the U.S.S.R.
Platonov AE, Beloborodov VB, Vershinina IV Medicine (Baltimore) 1993(6): 374-92
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Infectious diseases associated with complement deficiencies.
Figueroa JE, Densen P Clin Microbiol Rev 1991(3): 359-95
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1984
Complement deficiency states and infection: epidemiology, pathogenesis and consequences of neisserial and other infections in an immune deficiency.
Ross SC, Densen P Medicine (Baltimore) 1984(5): 243-73
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