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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 6
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Hb Alperton [β135(H13)Ala→Val] Shows Decreased Oxygen Affinity

Karin Zurbriggen Division of Haematology, University Children's Hospital, Zürich, Switzerland
,
Marlis Schmid Division of Haematology, University Children's Hospital, Zürich, Switzerland
,
Markus Schmugge Division of Haematology, University Children's Hospital, Zürich, Switzerland
,
Heinz Troxler Division of Clinical Chemistry and Biochemistry, University Children's Hospital, Zürich, Switzerland
&
Oliver Speer Division of Haematology, University Children's Hospital, Zürich, Switzerland; Zürich Center for Integrative Human Physiology, University of Zürich, Zürich, SwitzerlandCorrespondence[email protected]
Pages 498-502 | Received 14 Apr 2009, Accepted 05 Jun 2009, Published online: 03 Dec 2009

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Koumudi G. Godbole, Angalena Ramachandran, Ashwini S. Karkamkar & Ashwin B. Dalal. (2018) Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family. Hemoglobin 42:2, pages 141-142.
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Maria Marsella, Gianluca Salvagno, Bernadetta Dolcini, Alessandra Ferlini, Anna Ravani, Cornelis L. Harteveld, Piero C. Giordano & Caterina Borgna-Pignatti. (2014) Characterization of Hb Calvino (HBB: c.406G > A): A New Silent β-Globin Gene Variant Found in Coexistence with α-Thalassemia in a Family of African Origin. Hemoglobin 38:5, pages 369-372.
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Articles from other publishers (1)

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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