Early manifestation and recognition of C2 complement deficiency in the form of pyogenic infection in infancy
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1440-1754.2003.00128.x/fullpdf
Reference23 articles.
1. Complement deficiency and disease
2. Molecular Heterogeneity of C2 Deficiency
3. Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing.
4. Type II Human Complement C2 Deficiency
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