Identification of a novel termination codon mutation (TAA-->TAT, Term-->Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease

Blood. 1994 Jun 1;83(11):3418-20.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Base Sequence
  • Child
  • Codon*
  • Female
  • Globins / genetics*
  • Humans
  • Molecular Sequence Data
  • Mutation*
  • alpha-Thalassemia / genetics*

Substances

  • Codon
  • Globins