INHERITED STRUCTURAL VARIATION AND LINKAGE RELATIONSHIPS OF C7
- 1 June 1978
- journal article
- Published by Wiley in International Journal of Immunogenetics
- Vol. 5 (3) , 157-163
- https://doi.org/10.1111/j.1744-313x.1978.tb00641.x
Abstract
Three structural forms of C7 have been distinguished by isoelectric focusing. They are the products of three co-dominantly expressed alleles at an autosomal locus. The C7 locus is close to that for C6, but is not close to the HLA complex.Keywords
This publication has 18 references indexed in Scilit:
- Genetic Independence between the HL-A System and Deficits in the First and Sixth Components of ComplementTissue Antigens, 2008
- LINKAGE STUDIES WITH C6International Journal of Immunogenetics, 1977
- Mapping of the HLA locus controlling C2 structural variants and linkage disequilibrium between alleles C22 and Bw15European Journal of Immunology, 1976
- Genetic polymorphism of C4 in man and localisation of a structural C4 locus to the HLA gene complex of chromosome 6Nature, 1976
- Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.The Journal of Experimental Medicine, 1976
- Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies.Journal of Clinical Investigation, 1976
- EVIDENCE FOR LINKAGE BETWEEN HL-A HISTOCOMPATIBILITY GENES AND THOSE INVOLVED IN THE SYNTHESIS OF THE SECOND COMPONENT OF COMPLEMENTThe Journal of Experimental Medicine, 1974
- C3 polymorphism: Genetic linkage relationsClinical Genetics, 1974
- REACTIVE LYSIS: THE COMPLEMENT-MEDIATED LYSIS OF UNSENSITIZED CELLSThe Journal of Experimental Medicine, 1970
- Genetic polymorphism of the third component of human complement (C′3)Journal of Clinical Investigation, 1968