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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 1
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Short Communication

Two New α Chain Variants: Hb Die [α93(FG5)Val→Ala (α1)] and Hb Beziers [α99(G6)Lys→Asn (α1)]

Philippe Lacan Unité de Pathologie Moléculaire, Fédération de Biochimie et de Biologie Spé cialisée, Hôspital Edouard Herriot, 69437, Lyon Cedex 03, France
,
Martine Aubry Unité de Pathologie Moléculaire, Fédération de Biochimie et de Biologie Spé cialisée, Hôspital Edouard Herriot, 69437, Lyon Cedex 03, France
,
Nicole Couprie Laboratoire Marcel Mérieux, 69365, Lyon Cedex 07, France
&
Alain Francina Unité de Pathologie Moléculaire, Fédération de Biochimie et de Biologie Spé cialisée, Hôspital Edouard Herriot, 69437, Lyon Cedex 03, France
Pages 59-63 | Received 12 May 2003, Accepted 22 Sep 2003, Published online: 24 Aug 2009

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Rong-Yue Wang, Fan Jiang, Li-Li Xu & Dong-Zhi Li. (2021) Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation. Hemoglobin 45:2, pages 140-141.
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Mohamed S.M. Khalil, Adele T. Timbs, Shirley J. Henderson, Anna Schuh, Mohamed M. El-Khawanky & John M. Old. (2020) A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK. Hemoglobin 44:3, pages 195-200.
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Kamran Moradkhani, Jean Riou, Alain Francina, Henri Wajcman & Claude Prehu. (2008) Hb Gerland [α55(E4)Val→Ala]: A Mutation Found on the α1-Globin Gene. Hemoglobin 32:5, pages 478-484.
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Articles from other publishers (4)

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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Isabelle Zanella-Cleon, Michel Becchi, Philippe Lacan, Piero C Giordano, Henri Wajcman & Alain Francina. (2008) Detection of a Thalassemic α-Chain Variant (Hemoglobin Groene Hart) by Reversed-Phase Liquid Chromatography. Clinical Chemistry 54:6, pages 1053-1059.
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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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d'Artis Kancs. (2010) Variety Gains of Trade Integration in a Heterogeneous Firm Model. SSRN Electronic Journal.
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