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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Detalles Bibliográficos
Autores principales: Ki, Chang-Seok, Kim, Jong-Won, Kim, Hee-Jin, Choi, Sung-Min, Ha, Gyoung-Yim, Kang, Hee Jung, Kim, Won-Duck
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2005
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2808595/
https://www.ncbi.nlm.nih.gov/pubmed/15831990
http://dx.doi.org/10.3346/jkms.2005.20.2.220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2808595/
https://www.ncbi.nlm.nih.gov/pubmed/15831990
http://dx.doi.org/10.3346/jkms.2005.20.2.220

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