Clinical and molecular characterization of a rare 2.4 kb deletion causing α(+) thalassemia in a Chinese family

Blood Cells Mol Dis. 2012 Aug 15;49(2):83-4. doi: 10.1016/j.bcmd.2012.05.006. Epub 2012 Jun 2.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Asian People / genetics*
  • Child
  • Female
  • Heterozygote
  • Humans
  • Male
  • Pedigree
  • Sequence Analysis, DNA
  • Sequence Deletion*
  • alpha-Globins / genetics*
  • alpha-Thalassemia / genetics*

Substances

  • alpha-Globins