Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 3
87
Views
5
CrossRef citations to date
0
Altmetric
Original Article

A Novel β-Thalassemia Mutation in a Chinese family: IVS-II-203-205 (TCT>CC) (HBB: c.315+203TCT>CC)

, &
Pages 159-160 | Received 24 May 2018, Accepted 25 Jun 2018, Published online: 25 Sep 2018

References

  • Lai K, Huang G, Su L, et al. The prevalence of thalassemia in mainland China: evidence from epidemiological surveys. Sci Rep. 2017;7(1):920–931.
  • HbVar database [Internet]. Available from: http://globin.cse.psu.edu.
  • Danjou F, Anni F, Galanello R. β-Thalassemia: from genotype to phenotype. Haematologica. 2011;96(11):1573–1575.
  • Charoenkwan P, Sirichotiyakul S, Phusua A, et al. High-resolution melting analysis for prenatal diagnosis of β-thalassemia in northern Thailand. Int J Hematol. 2017;106:757–764.
  • Vinciguerra M, Passarello C, Leto F, et al. Coinheritance of a rare nucleotide substitution on the β-globin gene and other known mutations in the globin clusters: management in genetic counseling. Hemoglobin. 2016;40(4):231–235.
  • Azimi A, Alibakhshi R, Hayati H, et al. IVS-II-648/649 (–T) (HBB: c.316-202del) triggers a novel β-thalassemia phenotype. Hemoglobin. 2017;41(1):44–46.
  • George E, Jamal AR, Khalid F, et al. High performance liquid chromatography (HPLC) as a screening tool for classical β-thalassaemia trait in Malaysia. Malaysian J Med Sci. 2001;8(2):40–46.
  • Pornprasert S, Tookjai M, Punyamung M, et al. Proficiency testing program for Hemoglobin E, A2 and F analysis in Thailand using lyophilized hemoglobin control materials. Clin Chem Lab Med. 2018;56(4):602–608.
  • Jankovic L, Dimovski AJ, Sukarova E, et al. A new mutation in the β-globin gene (IVS II-850 G-C) found in a Yugoslavian β-thalassemia heterozygote. Haematologica. 1992;77(2):119–121.
  • Jiang F, Chen GL, Zhou JY, et al. First report of the rare IVS-II-705 (T>G) β-thalassemia mutation in a Chinese family. Hemoglobin. 2017;41(4–6):286–287.
  • Sahoo SS, Biswal S, Dixit M. Distinctive mutation spectrum of the HBB gene in an urban eastern Indian population. Hemoglobin. 2014;38(1):33–38.

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.