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

Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait

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Pages 291-292 | Received 11 Oct 2017, Accepted 18 Oct 2017, Published online: 18 Dec 2017

References

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  • Lacerra G, Scarano C, Lagona LF, et al. Genotype-phenotype relationship of the δ-thalassemia and Hb A2 variants: observation of 52 genotypes. Hemoglobin. 2010;34(5):407–423.
  • Jain S, Edison ES, Mathews V, Shaji RV. A novel δ-globin gene mutation (HBD: c.323G>A) masking the diagnosis of β-thalassemia: a first report from India. Int J Hematol. 2012;95(5):570–572.
  • Gray GR, Manson HE, Gu L-H, et al. Hb Lulu Island (α2β2107[G9]Gly→Asp)-β0-thalassemia (codon 15; TGG→TAG), a form of thalassemia intermedia. Am J Hematol. 1995;50(1):26–29.
  • Liu N, Xie XM, Zhou JY, et al. Analysis of δ-globin gene mutations in the Chinese population. Hemoglobin. 2013;37(1):85–93.

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