A familial dysfunction of the eighth component of complement (C8)
- 1 June 1980
- journal article
- research article
- Published by Elsevier in Clinical Immunology and Immunopathology
- Vol. 16 (2) , 180-191
- https://doi.org/10.1016/0090-1229(80)90202-0
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- INHERITED STRUCTURAL VARIATION AND LINKAGE RELATIONSHIPS OF C7International Journal of Immunogenetics, 1978
- Inherited Deficiency of the Seventh Component of Complement Associated with NephritisJournal of Clinical Investigation, 1978
- C8 deficiency in a family with xeroderma pigmentosumClinical Immunology and Immunopathology, 1977
- Absence of the Eighth Component of Complement in Association with Systemic Lupus Erythematosus-Like DiseaseJournal of Clinical Investigation, 1977
- Human deficiency of the eighth component of complement. The requirement of C8 for serum Neisseria gonorrhoeae bactericidal activity.Journal of Clinical Investigation, 1976
- Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA)Cytogenetic and Genome Research, 1976
- Hereditary deficiency of the seventh component of complement.Journal of Clinical Investigation, 1975
- LEUKOCYTE LOCOMOTION AND CHEMOTAXISThe Journal of Experimental Medicine, 1973
- HOMOZYGOUS DEFICIENCY OF C3 IN A PATIENT WITH REPEATED INFECTIONSThe Lancet, 1972
- Genetic polymorphism of the third component of human complement (C′3)Journal of Clinical Investigation, 1968