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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 3
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Original Article

Hb Brie Comte Robert [β36(C2)Pro→Ala]: A New Hemoglobin Variant with High Oxygen Affinity and Marked Hydrophobic Properties

H. Wajcman INSERM U 468, Hôpital Henri Mondor, 94010, Créteil, FranceCorrespondence[email protected]
,
J. Riou Department of Biochemistry, Hôpital Henri Mondor, 94010, Créteil, France
,
D. Promé Institut de Pharmacologic et de Biologie Structurale, CNRS, 31077, Toulouse, France
,
J. Kister INSERM U473, 94276 Le Kremlin-Bicetre Cedex, France
&
F. Galactéros Department of Biochemistry, Hôpital Henri Mondor, 94010, Créteil, France
Pages 281-286 | Received 20 Nov 1998, Accepted 20 Jan 1999, Published online: 07 Jul 2009

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Anna Maria Salzano, Virginia Carbone, Leonilde Pagano, Salvatore Buffardi, Carlo De Rosa & Piero Pucci. (2002) Hb VILA REAL [β36(C2)Pro → His] IN ITALY: CHARACTERIZATION OF THE AMINO ACID SUBSTITUTION AND THE DNA MUTATION. Hemoglobin 26:1, pages 21-31.
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Ioannis Papassotiriou, Joanne Traeger-Synodinos, Danielle Promé, Jean Kister, Christina Vrettou, Athina Xaidara, Michael Marden, Alexandra Stamoulakatou, Henri Wajcman & Emmanuel Kanavakis. (2001) Hb SITIA [β128(H6)Ala→Val]: AN UNSTABLE VARIANT WITH A SUBSTITUTION IN THE α1β1 INTERFACE. Hemoglobin 25:1, pages 45-56.
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Articles from other publishers (1)

Sonny O. Ang & Josef T. Prchal. 2007. Myeloproliferative Disorders. Myeloproliferative Disorders 297 319 .

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