Association between combined properdin and mannose-binding lectin deficiency and infection with Neisseria meningitidis

Author:

Bathum Lise,Hansen Heidi,Teisner Børge,Koch Claus,Garred Peter,Rasmussen Kirsten,Wang Palle

Publisher

Elsevier BV

Subject

Molecular Biology,Immunology

Reference24 articles.

1. Detection and quantitation of immune complexes with a rapid PEG-complement consumption method;Brandslund,1981

2. Double-Decker rocket immunoelectrophoresis for direct quantitation of complement C3 split products with C3d specificities in plasma;Brandslund;J. Immunol. Meth.,1981

3. Host genetic determinants of Neisseria meningitidis infections;Emonts;Lancet Infect. Dis.,2003

4. Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiency;Fijen;Clin. Exp. Immunol.,1995

5. Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange;Fredrikson;J. Immunol.,1996

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