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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).
- Spath, PJ (author)
- Sjoholm, AG (author)
- Fredrikson, GN (author)
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- Misiano, G (author)
- Scherz, R (author)
- Schaad, UB (author)
- Uhring-Lambert, B (author)
- Hauptmann, G (author)
- Westberg, J (author)
- Uhlen, M (author)
- Truedsson, L (author)
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- (creator_code:org_t)
- 1999
- 1999
- English.
- In: Clin Exp Immunol. ; 118, s. 278-
- Journal article (peer-reviewed)
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- Spath, PJ
- Sjoholm, AG
- Fredrikson, GN
- Misiano, G
- Scherz, R
- Schaad, UB
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- Uhring-Lambert, ...
- Hauptmann, G
- Westberg, J
- Uhlen, M
- Wadelius, C
- Truedsson, L
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- Clin Exp Immunol
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- Uppsala University
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