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Items: 4

1.
Properdin deficiency in a family with fulminant meningococcal infections.
A G Sjöholm, J H Braconier, C Söderström
Clin Exp Immunol. 1982 Nov; 50(2): 291–297.
PMCID:
PMC1536695
SummaryPage BrowsePDF–761K
2.
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
SummaryPage BrowsePDF–923K
3.
Characterization of the human properdin gene.
K F Nolan, S Kaluz, J M Higgins, D Goundis, K B Reid
Biochem J. 1992 Oct 1; 287(Pt 1): 291–297. doi: 10.1042/bj2870291
PMCID:
PMC1133157
SummaryPage BrowsePDF–1.6M
4.
Carrier detection in families with properdin deficiency by microsatellite haplotyping.
K Kölble, A J Cant, A C Fay, K Whaley, M Schlesinger, K B Reid
J Clin Invest. 1993 Jan; 91(1): 99–102. doi: 10.1172/JCI116207
PMCID:
PMC330001
SummaryPage BrowsePDF–770K

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