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Celeste Bento, Ana Catarina Oliveira, Joana Neves, Mariline Gameiro, Elizabete Cunha, Margarida Coucelo, Ricardo Marques Costa, José Barbot, Emilia Costa, Carlos Fernández-Lago & M. Leticia Ribeiro. (2012) Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a New α-Thalassemic Hemoglobin Variant Found in the Iberian Peninsula: Report of Six Cases. Hemoglobin 36:6, pages 517-525.
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Philippe Joly, Anton Szymanowicz, Marie-Jeanne Neyron, Abdellah Zine, Henri Wajcman & Alain Francina. (2010) Hb Charlieu [α106(G13)Leu→Pro (α1)]: A New Phenotypically Silent Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype. Hemoglobin 34:4, pages 366-373.
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Cornelis L. Harteveld, Florens G.A. Versteegh, Eduard H.G. van Leer, Jaap S. Starreveld, Peter J.M.J. Kok, Irene van Rooijen-Nijdam, Peter van Delft, Isabelle Zanella-Cleon, Michel Becchi, Henri Wajcman & Piero C. Giordano. (2007) Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Gene in Cis with a −α3.7 Thalassemia Deletion. Hemoglobin 31:3, pages 313-323.
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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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Piero C. Giordano, Sonja Zweegman, Nicole Akkermans, Sandra G.J. Arkesteijn, Peter van Delft, Florens G.A. Versteegh, Henri Wajcman & Cornelis L. Harteveld. (2007) The First Case of Hb Groene Hart [α119(H2)Pro→Ser, CCT→TCT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant. Hemoglobin 31:2, pages 179-182.
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Articles from other publishers (6)
Chris E. Cooper, Matthew Bird, XiaoBo Sheng, Ji-Won Choi, Gary G.A. Silkstone, Michelle Simons, Natalie Syrett, Riccardo Piano, Luca Ronda, Stefano Bettati, Gianluca Paredi, Andrea Mozzarelli & Brandon J. Reeder. (2021) Stability of Maleimide-PEG and Mono-Sulfone-PEG Conjugation to a Novel Engineered Cysteine in the Human Hemoglobin Alpha Subunit. Frontiers in Chemistry 9.
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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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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin
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Sean Lynch, Rebecca Stoltzfus & Rahul Rawat. (2016) Critical Review of Strategies to Prevent and Control Iron Deficiency in Children. Food and Nutrition Bulletin 28:4_suppl4, pages S610-S620.
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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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