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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 1
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Original

Hb Barika [α42(C7)Tyr→His (α2)] Leads to an α+-Thalassemia-like Syndrome

Claude Préhu INSERM U654 and Service de Biochimie, Hôpital Henri Mondor AP-HP, Créteil, France
,
Jean Riou INSERM U654 and Service de Biochimie, Hôpital Henri Mondor AP-HP, Créteil, France
&
Henri Wajcman INSERM U654 and Service de Biochimie, Hôpital Henri Mondor AP-HP, Créteil, FranceCorrespondence[email protected]
Pages 17-22 | Received 07 Jul 2006, Accepted 14 Jul 2006, Published online: 07 Jul 2009

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Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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Cornelis L. Harteveld, Willem C.H. van Helden, George L. Boxma, Peter van Delft, Margaretha Bakker-Verweij, Henri Wajcman, Isabelle Zanella-Cleon, Michel Becchi & Piero C. Giordano. (2007) Hb Zoetermeer: A New Mutation on the α2 Gene Inducing an Ala→Ser Substitution at Codon 21 is Possibly Associated with a Mild Thalassemic Phenotype. Hemoglobin 31:3, pages 325-332.
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