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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 2
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Miscellaneous Article

Identification of the Nucleotide Change (CAC→CGC) Responsible for Hb P-Galveston [β117(G19)His→Arg]

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Pages 165-167 | Received 15 Nov 2999, Accepted 25 Nov 1999, Published online: 07 Jul 2009

References

  • Schneider R. G., Haggard M. B. A new hemoglobin variant exhibiting anomalous electrophoretic behavior. Nature 1957; 180: 1486–1487
  • Schneider R. G., Alperin J. B., Brimhall B., Jones R. T. Hemoglobin P (α2β2117Arg): structure and properties. J. Lab. Clin. Med. 1969; 73: 616–622
  • Di Iorio E. E., Winterhalter K. H., Wilson K., Rosenmund A., Marti H. R. A Swiss family with Hemoglobin P Galveston β117Hisåg, including two patients with Hb P/β-thalassemia. Blüt 1975; 3151–68
  • Witkowska H. E., Bitsch F., Shackleton C. H.L. Expediting rare variant hemoglobin characterization by combined HPLC/electrospray mass spectrometry. Hemoglobin 1993; 17: 227–242
  • Ou C. N., Rognerud C. L. Rapid analysis of hemoglobin variants by cation-exchange HPLC. Clin. Chem. 1993; 39: 820–824

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