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Hemoglobin
international journal for hemoglobin research
Volume 41, 2017 - Issue 4-6
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Short Communication

A Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>T

, , , , & ORCID Icon
Pages 306-307 | Received 08 Aug 2017, Accepted 16 Sep 2017, Published online: 18 Dec 2017

References

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  • Akbari MT, Hamid M. Identification of α-globin chain variants a report from Iran. Arch Iran Med. 2012;15(9):564–567.
  • Zhou JY, Yan JM, Li J, Li DZ. First case of a compound heterozygosity for two nondeletional α-thalassemia mutations, Hb Constant Spring and Hb Quong Sze. Hemoglobin. 2016;40(3):210–212.
  • Bernini LF, Harteveld CL. α-Thalassaemia. Bailliére’s Clin Haematol. 1998;11(1):53–90.
  • He J, Song W, Yang J, et al. Next-generation sequencing improves thalassemia carrier screening among premarital adults in a high prevalence population: the Dai nationality, China. Genet Med. 2017;19(9):1022–1031.

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