One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain.

Y. J. Fei, T. A. Stoming, A. Kutlar, T. H. Huisman, G. Stamatoyannopoulos

Research output: Contribution to journalLetter

39 Scopus citations
Original languageEnglish (US)
Pages (from-to)1075-1077
Number of pages3
JournalBlood
Volume73
Issue number4
StatePublished - Mar 1 1989
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

Cite this

Fei, Y. J., Stoming, T. A., Kutlar, A., Huisman, T. H., & Stamatoyannopoulos, G. (1989). One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain. Blood, 73(4), 1075-1077.