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Hemoglobin
international journal for hemoglobin research
Volume 27, 2003 - Issue 2
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Original

The Mutation of Hb Turriff [α99(G6)Lys→Glu (AAG→GAG)] Is Carried by the α1‐Globin Gene in a Japanese (Hb Turriff‐I)

Teruo Harano Department of Biochemistry, Kawasaki Medical School, 577 Matsushima, Kurashiki, 701‐0192, Japan
,
Keiko Harano Department of Biochemistry, Kawasaki Medical School, 577 Matsushima, Kurashiki, 701‐0192, Japan
,
Yin‐Feng Hong Department of Biochemistry, Kawasaki Medical School, 577 Matsushima, Kurashiki, 701‐0192, Japan
,
Aung Myint Than Department of Biochemistry, Kawasaki Medical School, 577 Matsushima, Kurashiki, 701‐0192, Japan
,
Yoshimasa Suetsugu Department of Biochemistry, Kawasaki Medical School, 577 Matsushima, Kurashiki, 701‐0192, Japan
&
Kenzou Ohba Division of Geriatric Medicine, Nippon Medical School, Bunkyo‐Ku, Tokyo, Japan
Pages 123-127 | Received 28 Oct 2002, Accepted 23 Nov 2002, Published online: 07 Jul 2009

Citations (3)

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Read on this site (1)

Philippe Lacan, Martine Aubry, Nicole Couprie & Alain Francina. (2004) Two New α Chain Variants: Hb Die [α93(FG5)Val→Ala (α1)] and Hb Beziers [α99(G6)Lys→Asn (α1)]. Hemoglobin 28:1, pages 59-63.
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Articles from other publishers (2)

Xiang YuTodd L. MollanAndrew Butler, Andrew J. Gow, John S. OlsonMitchell J. Weiss. (2009) Analysis of human α globin gene mutations that impair binding to the α hemoglobin stabilizing protein. Blood 113:23, pages 5961-5969.
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Corinne Vasseur-Godbillon, Michael C. Marden, Piero Giordano, Henri Wajcman & Véronique Baudin-Creuza. (2006) Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome. Blood Cells, Molecules, and Diseases 37:3, pages 173-179.
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