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Two Novel Mutations in the C7 gene in a Korean Patient with Complement C7 Deficiency
Complement C7 deficiency is an autosomal recessive disorder well known to be associated with increased susceptibility to meningococcal infection and has mostly been reported in Caucasians. In the Korean population, no case of C7 deficiency has been reported to date. Recently we experienced an 11-yr-...
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| Main Authors: | , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
The Korean Academy of Medical Sciences
2005
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2808595/ https://ncbi.nlm.nih.gov/pubmed/15831990 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2005.20.2.220 |
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