Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype

Br J Haematol. 1991 Sep;79(1):117-9. doi: 10.1111/j.1365-2141.1991.tb08018.x.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Child
  • Child, Preschool
  • Codon / genetics
  • Female
  • Globins / genetics*
  • Humans
  • Infant
  • Male
  • Mutation / physiology*
  • Phenotype
  • Thalassemia / blood
  • Thalassemia / genetics*

Substances

  • Codon
  • Globins