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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 3
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Original Article

Hb Suan‐Dok [α109(G16)Leu→Arg; CTG→CGG (α2)] Described in a Patient of African Ancestry

Marlies E. Regtuijt Department of Internal Medicine, Leiden University Medical Center, Leiden, The Netherlands
,
Cornelis L. Harteveld Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL, Leiden, The Netherlands
,
Peter Van Delft Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL, Leiden, The Netherlands
,
Nicole Akkermans Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL, Leiden, The Netherlands
&
Piero C. Giordano Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL, Leiden, The Netherlands
, Ph.D.
Pages 173-176 | Received 16 Dec 2003, Accepted 26 Jan 2004, Published online: 24 Aug 2009

Citations (5)

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Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
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Kamran Moradkhani, Elodie Mazurier, Piero C. Giordano, Henri Wajcman & Claude Préhu. (2008) An α0-Thalassemia-Like Mutation: Hb Suan-Dok [α109(G16)Leu→Arg] Carried by a Recombinant −α3.7 Gene. Hemoglobin 32:4, pages 419-424.
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Cornelis L. Harteveld, Florens G.A. Versteegh, Peter J.M.J. Kok, Irene H. van Rooijen-Nijdam, Peter van Delft & Piero C. Giordano. (2006) Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype. Hemoglobin 30:3, pages 349-354.
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Articles from other publishers (2)

Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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Thanyachai Sura, Objoon Trachoo, Vip Viprakasit, Prin Vathesatogkit, Atchara Tunteeratum, Manisa Busabaratana, Raewadee Wisedpanichkij & Parttraporn Isarangkura. (2007) Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method. Annals of Hematology 86:9, pages 659-663.
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