Article
Molecular basis of the Kell (K1) phenotype.
Blood - 15 Feb 1995
Lee S, Wu X, Reid M, Zelinski T, Redman C
Abstract excerpt
K1 (K, Kell) is a strong immunogen; its antibodies can cause severe reactions if incompatible blood is transfused and may cause hemolytic disease of the newborn in sensitized mothers. K1 is a member of the Kell blood group system, which is complex, containing over 20 different antigens. Some of t...
Topics
- Amino Acid Sequence
- Base Sequence
- Consensus Sequence
- DNA
- DNA Primers
- Exons
- Genetic Variation
- Genotype
- Glycosylation
- Humans
- Kell Blood-Group System
- Methionine
- Molecular Sequence Data
- Phenotype
- Point Mutation
- Polymerase Chain Reaction
- Restriction Mapping
- Threonine