Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Drug Discovery,Biochemistry,Biotechnology
Reference70 articles.
1. Agnello, V., De Bracco, M.M., and Kunkel, H.G. (1972). Hereditary C2 deficiency with some manifestations of systemic lupus erythematosus. J Immunol 108, 837–840.
2. Alper, C.A., and Propp, R.P. (1968). Genetic polymorphism of the third component of human complement (C’3). J Clin Invest 47, 2181–2191.
3. Azen, E.A., and Smithis, O. (1968). Genetic polymorphism of C’3(beta1C-globulin) in human serum. Science 162, 905–907.
4. Bernard Cher, T.H., Chan, H.S., Klein, G.F., Jabkowski, J., Schadenböck-Kranzl, G., Zach, O., Roca, X., and Law, S.K. (2011). A novel 30 splice-site mutation and a novel gross deletion in leukocyte adhesion deficiency (LAD)-1. Biochem Biophys Res Commun 404, 1099–1104.
5. Blanchong, C.A., Chung, E.K., Rupert, K.L., Yang, Y., Yang, Z., Zhou, B., Moulds, J.M., and Yu, C.Y. (2001). Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4. Int Immunopharmacol 1, 365–392.
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