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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 4
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Short Communication

Hb Hekinan in a Taiwanese Subject: A G→T Substitution at Codon 27 of the α1-Globin Gene Abolishes an HaeIII Site

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Pages 495-498 | Received 28 Feb 2007, Accepted 06 Jun 2007, Published online: 07 Jul 2009

REFERENCES

  • Harano T, Harano K, Imai N, Ueda S, Seki M. An electrophoretically silent hemoglobin variant, Hb Hekinan [α27(B8)Glu→Asp] found in a Japanese. Hemoglobin 1988; 12(1)61–65
  • Merault G, Keclard L, Desfontaines L, Saint-Martin C, Blouquit Y, Rosa J, Galacteros F. Hemoglobin Hekinan [α227(B8)Glu→Aspβ2] detected in Guyana. Hemoglobin 1989; 13(4)397–402
  • Zhao W, Wilson JB, Webber BB, Kutlar A, Tamagnini GP, Kuam B, Huisman THJ. Hb Hekinan observed in three Chinese from Macau; identification of the GAG→GAT mutation in the α1-globin gene. Hemoglobin 1990; 14(6)627–635
  • Fucharoen S, Changtrakun Y, Ratanasiri T, Fucharoen G, Sanchaisuriya K. Complex interaction of Hb Hekinan [α27(B8)Glu→Asp] and Hb E [β26(B8)Glu→Lys] with a deletional α-thalassemia 1 in a Thai family. Eur J Haematol 2003; 70(5)304–309
  • Chang J-G, Yang T-Y, Perng L-I, Wang N-M, Peng C-T, Tsai C-H. Hb Siriraj: a G→A substitution at codon 7 of the β-globin chain creates an MboII cutting site. Hemoglobin 1999; 23(2)197–199
  • Chang J-G, Liu H-C, Shih M-C, Liu S-C, Chan W-L, Tsai F-J. Unstable Hb Perth in a Taiwanese subject: a T→C substitution at codon 32 of the β-globin gene creates an MspI site. Hemoglobin 2002; 26(1)91–94

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