Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 41, 2017 - Issue 3
118
Views
0
CrossRef citations to date
0
Altmetric
Short Communication

Coinheritance of High Oxygen Affinity Hb Helsinki [HBB: c.248A>T; β82(EF6)Lys→Met] with Hb H Disease

, , &
Pages 209-212 | Received 22 Apr 2017, Accepted 29 Jun 2017, Published online: 09 Aug 2017

References

  • Ikkala E, Koskela J, Pikkarainen P, et al. Hb Helsinki: a variant with a high oxygen affinity and a substitution at a 2,3-DPG binding site (β82[EF6]Lys→Met). Acta Haematologica. 1976;56(5):257–275.
  • Piel FB, Weatherall DJ. The α-Thalassemias. N Engl J Med. 2014;371(20):1908–1916.
  • Laosombat V, Viprakasit V, Chotsampancharoen T, et al. Clinical features and molecular analysis in Thai patients with Hb H disease. Ann Hematol. 2009;88(12):1185–1192.
  • Kham SKY, Quah TC, Loong AM, et al. A molecular epidemiologic study of thalassemia using newborns’ cord blood in a multiracial Asian population in Singapore. J Pediatr Hematol Oncol. 2004;26(12):817–819.
  • Eng B, Patterson M, Borys S, et al. PCR-based diagnosis of the Filipino (– –FIL) and Thai (– –THAI) α-thalassemia-1 deletions. Am J Hematol. 2000;63(1):54–56.
  • Chong SS, Boehm CD, Higgs DR, et al. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood. 2000;95(1):360–362.
  • Yap ZM, Sun KM, Teo CRL, et al. Evidence of differential selection for the –α3.7 and –α4.2 single α-globin gene deletions within the same population. Eur J Haematol. 2013;90(3):210–213.
  • 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. Nucl Acids Res. 2004;32(Database issue):D537–D541 (http://globin.cse.psu.edu/) (accessed 8 March 2017).
  • Schneider RG, Barwick RG. Hemoglobin mobility in citrate agar electrophoresis – its relationship to anion binding. Hemoglobin. 1982;6(2):199–208.
  • Weatherall DJ. The Thalassaemia Syndromes, 4th Ed. Oxford, Oxfordshire, UK: Blackwell Science Ltd., 2001.
  • Agarwal AM, Nussenzveig RH, Hoke C, et al. Identification of one or two α-globin gene deletions by isoelectric focusing electrophoresis. Am J Clin Pathol. 2013;140(3):301–305.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.