Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the Agamma -158 C>T mutation in gamma-globin gene transcription

Blood Cells Mol Dis. 2008 Nov-Dec;41(3):263-4. doi: 10.1016/j.bcmd.2008.05.009. Epub 2008 Aug 20.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Female
  • Fetal Hemoglobin / genetics*
  • Hemoglobins, Abnormal / genetics*
  • Heterozygote
  • Humans
  • Male
  • Point Mutation
  • beta-Thalassemia / genetics*
  • gamma-Globins / genetics*

Substances

  • Hemoglobins, Abnormal
  • gamma-Globins
  • hemoglobin Sabine
  • Fetal Hemoglobin