HB f-cobb OR α2aγ237(c3)TRP→GLY

S. S. Chen, B. B. Webber, A. Kutlar, J. B. Wilson, T. H.J. Huisman

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

An electrophoretically slow-moving hemoglobin (Hb) component was found in the red cell lysate from a Caucasian newborn (50777) which is characterized by a Trp→Gly substitution at position 37 (C3) of the Aγ chain. Since such a replacement has not been observed before, the variant was named F-Cobb after the county of residence.

Original languageEnglish (US)
Pages (from-to)617-619
Number of pages3
JournalHemoglobin
Volume9
Issue number6
DOIs
StatePublished - Jan 1 1985

ASJC Scopus subject areas

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

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    Chen, S. S., Webber, B. B., Kutlar, A., Wilson, J. B., & Huisman, T. H. J. (1985). HB f-cobb OR α2aγ237(c3)TRP→GLY. Hemoglobin, 9(6), 617-619. https://doi.org/10.3109/03630268508997043