Article
A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype.
The Journal of clinical investigation - 1 Oct 1992
Fasano M B, Winkelstein J A, LaRosa T, Bias W B, McLean R H
Abstract excerpt
The fourth component of complement (C4) is encoded by two closely linked genes (C4A and C4B) within the MHC. Null alleles at either locus (C4AQ0 or C4BQ0) are relatively common, occurring at the C4A locus in approximately 10% of normal individuals and at the C4B locus in approximately 16% of norm...
Topics
- Blotting, Southern
- Child
- Chromosome Mapping
- Complement C4
- Haplotypes
- Humans
- Male
- Phenotype
- Recombination, Genetic
- Steroid 21-Hydroxylase
