HB f-cobb OR α2aγ237(c3)TRP→GLY

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

Research output: Contribution to journalArticle

7 Citations (Scopus)

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

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Hemoglobins
Substitution reactions
Cells
hemoglobin A(0)

ASJC Scopus subject areas

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

Cite this

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

HB f-cobb OR α2aγ237(c3)TRP→GLY. / Chen, S. S.; Webber, B. B.; Kutlar, Abdullah; Wilson, J. B.; Huisman, T. H J.

In: Hemoglobin, Vol. 9, No. 6, 01.01.1985, p. 617-619.

Research output: Contribution to journalArticle

Chen, SS, Webber, BB, Kutlar, A, Wilson, JB & Huisman, THJ 1985, 'HB f-cobb OR α2aγ237(c3)TRP→GLY', Hemoglobin, vol. 9, no. 6, pp. 617-619. https://doi.org/10.3109/03630268508997043
Chen SS, Webber BB, Kutlar A, Wilson JB, Huisman THJ. HB f-cobb OR α2aγ237(c3)TRP→GLY. Hemoglobin. 1985 Jan 1;9(6):617-619. https://doi.org/10.3109/03630268508997043
Chen, S. S. ; Webber, B. B. ; Kutlar, Abdullah ; Wilson, J. B. ; Huisman, T. H J. / HB f-cobb OR α2aγ237(c3)TRP→GLY. In: Hemoglobin. 1985 ; Vol. 9, No. 6. pp. 617-619.
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