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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 4
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Short Communications

Hb Koya Dora [α142, Term→Ser (TAA>TCA in α2)]: A Rare Mutation of the α2 Gene Stop Codon Associated with α-Thalassemia

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Pages 402-405 | Received 19 Jan 2010, Accepted 25 Jan 2010, Published online: 19 Jul 2010

REFERENCES

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  • Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537-D541 (http://globin.bx.cse.psu.edu/hbvar).
  • Brennan SO, Mathews JRD. Hb Auckland [α87(F8)His→Asn]: a new mutation of the proximal histidine identified by electrospray mass spectrometry. Hemoglobin. 1997;21(5):393–403.
  • Brennan SO, Owen MC, Chan T, Ruscova A. Novel hemoglobin α chain elongation resulting from a 15-residue insertion and tandem duplication of the F helix. Clin Biochem. 2008;41(14–15):1156–1161.

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