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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 3
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Original Article

Hb Diamant [α119(H2)Pro→Leu]: A New Variant with a Modification at the α1β1 Interface

C. Préhu INSERM U 468, 94010, Créteil, France; Department of Biochemistry Hôpital, Henri Mondor AP-HP, 94010, Créteil, France
,
J. Riou Department of Biochemistry Hôpital, Henri Mondor AP-HP, 94010, Créteil, France
,
C. Godart Department of Biochemistry Hôpital, Henri Mondor AP-HP, 94010, Créteil, France
,
M. Bost Hématologic Biologique, Centre Hospitalier Universitaire de Grenoble, 38043, Grenoble, Cedex 9, France
,
C. Barro Hématologic Biologique, Centre Hospitalier Universitaire de Grenoble, 38043, Grenoble, Cedex 9, France
,
D. Promé Université Paul Sabatier, 31062, Toulouse, Cedex 4, France
,
J. Kister INSERM U 473, 94276 Le Kremlin-Bicětre, Cedex, France
,
F. Galactéros Department of Biochemistry Hôpital, Henri Mondor AP-HP, 94010, Créteil, France
&
H. Wajcman INSERM U 468, 94010, Créteil, FranceCorrespondence[email protected]
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Pages 249-252 | Received 24 Jan 2000, Accepted 09 Mar 2000, Published online: 07 Jul 2009

Citations (6)

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Cornelis L. Harteveld, Peter van Delft, Rob Plug, Florens G.A. Versteegh, Balt Hagen, Irene van Rooijen, Peter J.M.J. Kok, Henri Wajcman, Jean Kister & Piero C. Giordano. (2002) Hb GROENE HART: A NEW Pro→Ser AMINO ACID SUBSTITUTION AT POSITION 119 OF THE α1-GLOBIN CHAIN IS ASSOCIATED WITH A MILD α-THALASSEMIA PHENOTYPE. Hemoglobin 26:3, pages 255-260.
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Articles from other publishers (5)

Giovanni Antonello, Carlo Lo Monaco, Patrizia Napoli, Daniela Solimando, Cristina Curcio, Giuseppina Barberio, Sauro Maoggi, Giovanni Ivaldi & Marco Nigra. (2022) Two co-inherited hemoglobin variants revealed by capillary electrophoresis during quantification of glycated hemoglobin. Clinical Chemistry and Laboratory Medicine (CCLM) 60:6, pages 886-890.
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Karen G. Scheps, Marcia A. Hasenahuer, Gustavo Parisi, Héctor M. Targovnik & María S. Fornasari. (2019) Curating the gnomAD database: Report of novel variants in the globin‐coding genes and bioinformatics analysis. Human Mutation 41:1, pages 81-102.
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Corinne Vasseur, Elisa Domingues-Hamdi, Thomas Brillet, Michael C. Marden & Véronique Baudin-Creuza. (2009) The α-hemoglobin stabilizing protein and expression of unstable α-Hb variants. Clinical Biochemistry 42:18, pages 1818-1823.
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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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