Compound heterozygote condition in beta thalassemia major due to a novel single nucleotide deletion (-T) at codon 69 in association with IVS 1-5 (G>C) mutation

Int J Lab Hematol. 2012 Aug;34(4):e7-9. doi: 10.1111/j.1751-553X.2012.01412.x. Epub 2012 Mar 12.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Base Sequence
  • Heterozygote
  • Humans
  • Infant
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Sequence Deletion*
  • beta-Thalassemia / genetics*