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Hemoglobin
international journal for hemoglobin research
Volume 37, 2013 - Issue 2
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Short Communication

Codon 62 (GTG>GCG, Val→Ala) (α1) (HBA1: c.188T>C) Causing Nondeletional α-Thalassemia in a Chinese Family

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Pages 188-191 | Received 10 Oct 2012, Accepted 06 Nov 2012, Published online: 07 Mar 2013

REFERENCES

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  • Lal A, Goldrich ML, Haines DA, Azimi M, Singer ST, Vichinsky EP. Heterogeneity of Hemoglobin H disease in childhood. N Engl J Med. 2011;364(8):710–718.
  • Tang HS, Zhou JY, Xie XM, Li R, Liao C, Li DZ. Screening for common nondeletional α-thalassemias in Chinese newborns by determination of Hb Bart’s using the Sebia Capillarys 2 electrophoresis system. Hemoglobin. 2012;36(2):196–199.
  • Wilson JB, Webber BB, Kutlar A, . Hb Evans or α262(E11)Val→Metβ2; an unstable hemoglobin causing a mild hemolytic anemia. Hemoglobin. 1989;13(6):557–566.
  • Traeger-Synodinos J, Harteveld CL, Kanavakis E, Giordano PC, Kattamis C, Bernini LF. Hb Aghia Sophia [α62(E11)Val→0 (α1)], an “in-frame” deletion causing α-thalassemia. Hemoglobin. 1999;23(4):317–324.

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