A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous G γ(A γδβ)0 -thalassemia

Am J Hematol. 2021 Jun 1;96(6):E189-E193. doi: 10.1002/ajh.26148. Epub 2021 Mar 22.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Consanguinity
  • Fetal Hemoglobin / analysis
  • Homozygote
  • Humans
  • Male
  • Multigene Family
  • Pedigree
  • Phenotype
  • Sequence Deletion*
  • beta-Globins / deficiency
  • beta-Globins / genetics*
  • beta-Thalassemia / blood
  • beta-Thalassemia / genetics*
  • delta-Globins / deficiency
  • delta-Globins / genetics*
  • gamma-Globins / deficiency
  • gamma-Globins / genetics*

Substances

  • beta-Globins
  • delta-Globins
  • gamma-Globins
  • Fetal Hemoglobin