Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G...

Por Späth, P J, Sjöholm, A G, Nordin Fredrikson, G, Misiano, G, Scherz, R, Schaad, U B, Uhring-Lambert, B, Hauptmann, G, Westberg, J, Uhlén, M, Wadelius, C, Truedsson, L
Publicado em 1999