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Properdin deficiency in a large Swiss family: identification of a stopcodon in the properdin gene, and association of meningococcal disease withlack of the IgG2 allotype marker G2m(n).
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1999 (English)In: Clin Exp Immunol, Vol. 118, 278- p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
1999. Vol. 118, 278- p.
URN: urn:nbn:se:uu:diva-51554OAI: oai:DiVA.org:uu-51554DiVA: diva2:79463
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-14

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