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Heterozygous C8β complement deficiency does not predispose to meningococcal disease
We have identified 42 Russian patients with homozygous C8β complement component deficiency, all of whom had experienced at least one episode of systemic meningococcal disease. About 90% of these individuals have a C → T exchange in exon 9, leading to a premature stop codon. If, like the homozygous-d...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Blackwell Science Inc
1997
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1904676/ https://ncbi.nlm.nih.gov/pubmed/9182898 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2249.1997.3711263.x |
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