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

First Report of Hb Kent [β37(C3)Trp→Cys (TGG>TGC) HBB: c.114G>C] in a Chinese Family

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Pages 283-285 | Received 26 Jul 2017, Accepted 26 Aug 2017, Published online: 18 Oct 2017

References

  • Hoyer JD, Kaur P, Kozak EA, et al. Five variants of the β-globin gene without clinical or hematological effects: Hb Maryland [β47(CD6)Asp→His], Hb Kent [β37(C3)Trp→Cys], Hb Visayan [β136(H14)Gly→Cys], Hb Cutlerville [β138(H16)Ala→Val] and Hb Hornchurch [β43(CD2)Glu→Lys]. Hemoglobin. 2008;32(5):471–477.
  • Brennan SO, King RI, Florkowski CM. β37Trp→Cys mutation leads to multiple new hemoglobin species in red cells. Clin Biochem. 2012;45(3):259–263.
  • Liu YT, Old JM, Miles K, et al. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol. 2000;108(2):295–299.
  • Lau YL, Chan LC, Chan YY, et al. Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong – implications for population screening. N Engl J Med. 1997;336(18):1298–1301.

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