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24138.
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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 G2m(n). [electronic resource] by
- Späth, P J
- Sjöholm, A G
- Fredrikson, G N
- Misiano, G
- Scherz, R
- Schaad, U B
- Uhring-Lambert, B
- Hauptmann, G
- Westberg, J
- Uhlén, M
- Wadelius, C
- Truedsson, L
Producer: 19991122
In:
Clinical and experimental immunology vol. 118
Availability: No items available.
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24139.
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