Article
Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene.
Blood - 1 Apr 1997
Avent N D, Martin P G, Armstrong-Fisher S S, Liu W, Finning K M, Maddocks D, Urbaniak S J
Abstract excerpt
The human blood group Rh antigens are expressed by proteins encoded by a pair of highly homologous genes located at chromosome 1p34-36. One of the genes (RHCE) encodes Rh CcEe antigens, while the other (RHD) the D antigen. Point mutations in the RHCE gene generate the C/c and E/e polymorphisms, w...
Topics
- Amino Acid Sequence
- Base Sequence
- Chromosome Deletion
- Chromosomes, Human, Pair 1
- Cloning, Molecular
- Genes
- Genetic Variation
- Humans
- Introns
- Molecular Sequence Data
- Phenotype
- Point Mutation
- Polymerase Chain Reaction
- Rh-Hr Blood-Group System
- Terminator Regions, Genetic