A null allele caused by a four-base-pair duplication within the RHCE gene encoding a D- - phenotype

Transfusion. 2021 Mar;61(3):E23-E25. doi: 10.1111/trf.16211. Epub 2020 Dec 3.
No abstract available

Publication types

  • Case Reports
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Alleles
  • Asian People
  • Exons
  • Humans
  • Male
  • Mutagenesis, Insertional
  • Phenotype
  • Rh-Hr Blood-Group System / blood*
  • Rh-Hr Blood-Group System / genetics*
  • Rh-Hr Blood-Group System / immunology

Substances

  • RHCE protein, human
  • Rh-Hr Blood-Group System