Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia

Blood Cells Mol Dis. 2009 Sep-Oct;43(2):158-60. doi: 10.1016/j.bcmd.2009.05.006. Epub 2009 Jul 3.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Child, Preschool
  • Female
  • Glucosephosphate Dehydrogenase / genetics
  • Glucosephosphate Dehydrogenase Deficiency / genetics
  • Homozygote
  • Humans
  • Iran
  • Male
  • Pedigree
  • alpha-Globins / genetics*
  • beta-Globins / genetics*
  • beta-Thalassemia / genetics*

Substances

  • alpha-Globins
  • beta-Globins
  • Glucosephosphate Dehydrogenase