Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 2
83
Views
0
CrossRef citations to date
0
Altmetric
Short Communications

α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]

, &
Pages 205-207 | Received 24 Oct 2011, Accepted 12 Nov 2011, Published online: 29 Feb 2012

REFERENCES

  • Waye JS, Chui DHK. The α-globin gene cluster: genetics and disorders. Clin Invest Med. 2001;24(2):103–109.
  • 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.cse.psu.edu).
  • Dodé C, Rochette J, Krishnamoorthy R. Locus assignment of the human α-globin mutations by selective amplification and direct sequencing. Br J Haematol. 1990;76(2):275–281.
  • Khajavi M, Inoue K, Lupski JR. Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease. Eur J Hum Genet. 2006;14(10):1074–1081.
  • Chui DHK, Fucharoen S. Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood. 2003;101(3):791–800.

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.