A new hemoglobin variant in Hungary: Hb savaria-α49 (CE7) ser+arg

J. G. Szelényi, M. Horányi, J. Földi, J. Hudacsek, L. István, S. R. Hollán

Research output: Contribution to journalArticle

18 Citations (Scopus)


A hemoglobin variant of slow electrophoretic mobility has been demonstrated in a Hungarian female patient. The abnormal component amounted to about 30% and proved to be a new hemoglobin variant, α49 (CE7) Ser+Arg, which has been named Hb Savaria.

Original languageEnglish
Pages (from-to)27-38
Number of pages12
Issue number1
Publication statusPublished - Jan 1 1980

ASJC Scopus subject areas

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

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