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Hemoglobin
international journal for hemoglobin research
Volume 18, 1994 - Issue 4-5
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Original Article

A New β Chain Variant, Hb Tyne [β5(A2)Pro->ser]

J. V. Langdown Department of Haematology Addenbrookes, National Health Service Trust Cambridge, CB2 2QQ, England
,
D. Williamson Department of Haematology, University of Cambridge Medical Research Council Centre Cambridge, CB2 2QH, England
,
C. H. Beresford Department of Clinical Biochemistry, The Royal Victoria Infirmary, Newcastle, Upon Tyne, NE1 4LP, England
,
I. Gibb Department of Clinical Biochemistry, The Royal Victoria Infirmary, Newcastle, Upon Tyne, NE1 4LP, England
,
R. Taylor Department of Clinical Biochemistry, The Royal Victoria Infirmary, Newcastle, Upon Tyne, NE1 4LP, England
&
R. Deacon-Smith Department of Haematology Poole, Hospital National Health Service Trust Poole, Dorset, BH15 2JB, England
Pages 333-336 | Received 01 Dec 1993, Accepted 15 Apr 1994, Published online: 07 Jul 2009

Citations (11)

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Philippe Joly, Caroline Garcia, Philippe Lacan, Nicole Couprie & Alain Francina. (2011) Two New Hemoglobin Variants: Hb Aix-Les-Bains [β5(A2)Pro→Leu; HBB:c.17 C>T] and Hb Dubai [α122(H5)His→Leu (α2); HBA2:c.368 A>T]. Hemoglobin 35:2, pages 147-151.
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M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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Articles from other publishers (8)

Beverley M. Pullon & Stephen O. Brennan. (2017) Two Familial Cases of Hb Tyne Confirm Instability as Cause of Low Expression. Thalassemia Reports 7:1, pages 6504.
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Tânia Carlice-dos-Reis, Jaime Viana, Fabiano Cordeiro Moreira, Greice de Lemos Cardoso, João Guerreiro, Sidney Santos & Ândrea Ribeiro-dos-Santos. (2017) Investigation of mutations in the HBB gene using the 1,000 genomes database. PLOS ONE 12:4, pages e0174637.
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Jeanne M. Rhea & Ross Molinaro. (2014) Pathology Consultation on HbA1c Methods and Interferences. American Journal of Clinical Pathology 141:1, pages 5-16.
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Juan R. Alvarez-Dominguez, Olga Amosova & Jacques R. Fresco. (2013) Self-catalytic DNA Depurination Underlies Human β-Globin Gene Mutations at Codon 6 That Cause Anemias and Thalassemias. Journal of Biological Chemistry 288:16, pages 11581-11589.
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Giuseppina Lacerra, Clelia Scarano, Gennaro Musollino, Rosario Testa, Romeo Prezioso, Daniela G. Caruso, Laura F. Lagona, Emilia Medulla, Maria G. Friscia, Carlo Gaudiano & Clementina Carestia. (2009) HbA2-Partinico or δ(A2)Pro→Thr, a new genetic variation in the δ-globin gene in cis to the β+ thal IVS-I-110 G>A, and the heterogeneity of δ-globin alleles in double heterozygotes for β- and δ-globin gene defects. Annals of Hematology 89:2, pages 127-134.
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J. H. DeVries, F. J. Snoek & R. J. Heine. (2004) Persistent poor glycaemic control in adult Type 1 diabetes. A closer look at the problem. Diabetic Medicine 21:12, pages 1263-1268.
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Emmanuel Bissé, Claude Schauber, Nathalie Zorn, Thomas Epting, Antonin Eigel, Alain Van Dorsselaer, Heinrich Wieland, Jean Kister & Laurent Kiger. (2003) Hemoglobin Görwihl [α2β25(A2)Pro→Ala], an Electrophoretically Silent Variant with Impaired Glycation. Clinical Chemistry 49:1, pages 137-143.
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Ian Gibb, Angela Parnham, Michele Fonfrède & Freddy Lecock. (1999) Multicenter Evaluation of Tosoh Glycohemoglobin Analyzer. Clinical Chemistry 45:10, pages 1833-1841.
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