Deletion of Exons 3 through 5 of ABCG2 causes the Jr(a-) phenotype in a West African woman

Transfusion. 2015 Nov;55(11):2766-7. doi: 10.1111/trf.13223. Epub 2015 Jul 14.
No abstract available

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • ATP-Binding Cassette Transporters / genetics*
  • Alleles
  • Anemia, Sickle Cell / genetics
  • Black People
  • Exons / genetics*
  • Female
  • Humans
  • Neoplasm Proteins / genetics*
  • Polymerase Chain Reaction

Substances

  • ABCG2 protein, human
  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • ATP-Binding Cassette Transporters
  • Neoplasm Proteins