HB monroe or α2β230(b12)ARG→THR, a variant associated with βthalassemia due to a g→c substitution adjacent to the donor splice site of the first intron

J. M. Gonzalez-Redondo, T. A. Stoming, F. Kutlar, A. Kutlar, H. Hu, J. B. Wilson, T. H.J. Huisman

Research output: Contribution to journalArticlepeer-review

33 Scopus citations
Original languageEnglish (US)
Pages (from-to)67-74
Number of pages8
Issue number1
StatePublished - 1989

ASJC Scopus subject areas

  • Hematology
  • Genetics(clinical)
  • Clinical Biochemistry
  • Biochemistry, medical

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