Article
Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type.
Blood - 15 Jul 1998
Chérif-Zahar B, Matassi G, Raynal V, Gane P, Mempel W, Perez C, Cartron J P
Abstract excerpt
The deficiency of Rh proteins on the red blood cells from individuals of the Rhnull amorph type may be the result of homozygosity for a silent allele at the RH locus. This phenotype is also associated with the lack or reduced expression of glycoproteins (Rh50, CD47, LW, and glycophorin B), which...
Topics
- Alleles
- Amino Acid Sequence
- Blood Proteins
- Glycoproteins
- Humans
- Molecular Sequence Data
- Mutation
- Polymerase Chain Reaction
- Rh-Hr Blood-Group System
