- Two Novel Mutations in the C7 gene in a Korean Patient with Complement C7 Deficiency
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Ki CS, Kim JW, Kim HJ, Choi SM, Ha GY, Kang HJ, Kim WD
- KMID: 1095193
- J Korean Med Sci.
- 2005 Apr;20(2):220-224.
- doi: 10.3346/jkms.2005.20.2.220
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,... -
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