Author:
Minta Joe O.,Movat Henry Z.
Publisher
Springer Berlin Heidelberg
Reference264 articles.
1. Abramson, N., Alper, C.A., Lachmann, P.J., Rosen, F.S., Jandl, J.H.: Deficiency of C3b inactivator in man. J. Immunol. 107, 19–27 (1971)
2. Agnello, V., Koffler, D., Eisenberg, J.W., Winchester, R.J., Kunkel, H.G.: C1q precipitins in sera of patients with systemic lupus erythematosus and other hypocomplementemic states: characterization of high and low molecular weight types. J. Exp. Med. 134, 228S–255S (1971)
3. Agnello, V., de Brancco, M.M.E., Kunkel, H.G.: Hereditary C2 deficiency with some manifestations of systemic lupus erythematosus. J. Immunol. 108, 837–840 (1972)
4. Alper, C.A.: Inherited structural polymorphism in human C2, evidence for genetic linkage between C2 and Bf. J. Exp. Med. 144, 1111–1115 (1976)
5. Alper, C.A., Rosen, F.S.: Genetics of the complement system. Adv. Hum. Genet. 7, 141–188 (1976)
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