A C4 variant found in about 5% of the population is described. The fast-moving part of this variant is governed by an allele (Fx) codominant to F. The Fx allele is in very strong linkage disequilibrium with HLA-B17 as the linkage disequilibrium parameter accounted for nearly 100% of the haplotype fr
β¦ LIBER β¦
Genetic defects of complement in man
β Scribed by Lachmann, Peter J. ;Rosen, Fred S.
- Publisher
- Springer
- Year
- 1978
- Tongue
- English
- Weight
- 973 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0344-4325
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Genetic studies of complement C4 in man
β
G. B. Petersen; Inger Juncker Sørensen; Lisbeth Buskjær; L. U. Lamm
π
Article
π
1979
π
Springer
π
English
β 698 KB
Inherited deficiencies of complement com
β
Chester A. Alper
π
Article
π
1987
π
Elsevier Science
π
English
β 540 KB
Inherited deficiencies of complement pro
β
Alper, Chester A. ;Rosen, Fred S.
π
Article
π
1984
π
Springer
π
English
β 745 KB
Complementation of a dnaC initiation def
β
Projan, Steven J. ;Wechsler, James A.
π
Article
π
1981
π
Springer
π
English
β 395 KB
The dnaC28 mutant, CT28-3b, is an initiation defective dnaC strain. Extracts of the mutant failed to synthesize DNA in vitro when the strain was incubated at the restrictive temperature for two generation times prior to preparation of the extract. Addition of a complementing extract from a Col-E1::d
Genetic polymorphism of the complement C
β
K. Tokunaga; C. Araki; T. Juji; K. Omoto
π
Article
π
1981
π
Springer
π
English
β 313 KB
Defective complement activity in chronic
β
Margo E. Heath; Bruce D. Cheson
π
Article
π
1985
π
John Wiley and Sons
π
English
β 748 KB