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Hemoglobin
international journal for hemoglobin research
Volume 14, 1990 - Issue 5
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Original Article

Hb Sun Prae or α213o(H13)Ala → Proβ2 A New Unstable Variant Occurring In Low Quantities

M. Harkness Departments of Pediatrics and Medicine Clinical Sciences Center, University of Wisconsin, Madison, WI, 53792, USA
,
D. R. Harkness Departments of Pediatrics and Medicine Clinical Sciences Center, University of Wisconsin, Madison, WI, 53792, USA
,
F. Kutlar Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
A. Kutlar Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
J. B. Wilson Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
B. B. Webber Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
J. F. Codrington Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
T. H.J. Huisman Department of Cell and Molecular Biology Laboratory of Protein Chemistry, Medical College of Georgia, Augusta, GA, 30912-2100, USA
 show all
Pages 479-489 | Received 01 Dec 1989, Accepted 20 Mar 1990, Published online: 07 Jul 2009

Citations (34)

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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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Samaneh Farashi, Nooshin Bayat, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Hossein Najmabadi & Azita Azarkeivan. (2016) Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology 9:1, pages 107-113.
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Ahmad Tamaddoni, Valeh Hadavi, Nima Hafezi Nejad, Atefeh Khosh-Ain, Rita Siami, Jalil Aghai-Meibodi, Navid Almadani, Christian Oberkanins, Hai-Yang Law & Hossein Najmabadi. (2009) α-Thalassemia Mutation Analyses in Mazandaran Province, North Iran. Hemoglobin 33:2, pages 115-123.
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Gargi Bhattacharya, Anjali A. Sarkar, Debasish Banerjee, Sarmila Chandra, Manikanchan Das & Uma B. Dasgupta. (2008) Polymerase Chain Reaction-Based Search for Two α-Globin Gene Mutations in India. Hemoglobin 32:5, pages 485-490.
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Philippe Joly, Brigitte Pégourié, Stéphane Courby, Claire Barro, Gérard Besson, Laura Cohen, Caroline Garcia & Alain Francina. (2008) Two New α-Thalassemia Point Mutations that are Undetectable by Biochemical Techniques. Hemoglobin 32:4, pages 411-417.
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Kim L. McBride, Karen Snow, Kathleen S. Kubik, Virgil F. Fairbanks, James D. Hoyer, Robert B. Fairweather, Sara Chaffee & William H. Edwards. (2001) Hb DARTMOUTH [α66(E15)Leu → Pro (α2) (CTG → CCG)]: A NOVEL α2-GLOBIN GENE MUTATION ASSOCIATED WITH SEVERE NEONATAL ANEMIA WHEN INHERITED IN TRANS WITH SOUTHEAST ASIAN α-THALASSEMIA-1. Hemoglobin 25:4, pages 375-382.
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T. H.J. Huisman & M. F.H. Carver. (1998) The Thalassemia Repository (Ninth Edition; Part II). Hemoglobin 22:3, pages 287-310.
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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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P. J. Ho, J. Rochette, D. C. Rees, C. A. Fisher, E. R. Huehns, A. M. Will & S. L. Thein. (1996) Hb Sun Prairie: Diagnostic Pitfalls in Thalassemic Hemoglobinopathies. Hemoglobin 20:2, pages 103-112.
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. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
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. (1993) Variants of the Alpea Chain. Hemoglobin 17:2, pages 89-177.
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L-H. Gu, J. B. Wilson, T. P. Molchanova, K. M. McKie, V. C. McKie & T. H. J. Huisman. (1993) Three Sickle Cell Anemia Patients Each with a Different α Chain Variant. Diagnostic Complications. Hemoglobin 17:4, pages 295-301.
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. (1992) Variants of the Alpha Chain. Hemoglobin 16:3, pages 127-213.
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E. George, H-J. Li, Y-J. Fei, A. L. Reese, E. Baysal, B. Cepreganova, J. B. Wilson, L-H. Gu, J. F. Nechtman, T. A. Stoming, J-C. Liu, J. F. Codrington & T. H. J. Huisman. (1992) Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia. Hemoglobin 16:1-2, pages 51-66.
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. (1991) International hemoglobin information center: Variants of the alpha chain. Hemoglobin 15:3, pages 139-217.
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Y-C. Gu, L-H. Gu, J. B. Wilson, B. Cepreganova, M. Ramachandran, E. L.D. Walker, T. H. J. Huisman & P. Potitong. (1991) Hb Westmead [α122(H5)HIS→GLN], Hb E [β26(B8)6Ll→LYS], and α-Thamssemia-2 (3.7 KB Deletion) in a Laotian Family. Hemoglobin 15:4, pages 297-302.
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R. B. Gupta, R. S. Tiwary, P. L. Pande, F. Kutlar, C. Öner, R. Öner & T. H. J. Huisman. (1991) Hemoglobinopathies Among the Gond Tribal Groups of Central India; Interaction of α- and β-Thalassemia with β Chain Variants. Hemoglobin 15:5, pages 441-458.
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W. Zhao, J. B. Wilson, B. B. Webber, A. Kutlar, G. P. Tamagnini, B. Kuan & T. H. J. Huisnan. (1990) Hb Hekinan Observed in Three Chinese from Macau; Identification of the Gag→Gat Mutation in the αl-Globin Gene. Hemoglobin 14:6, pages 627-635.
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Articles from other publishers (15)

Ankur Jain, Pooja Prasad, Sumita Chaudhry, D.K. Gupta & Sumita Saluja. (2021) Hb Sun Prairie: A rare cause of chronic hemolysis in an Indian patient. Hematology/Oncology and Stem Cell Therapy 14:3, pages 257-259.
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Paloma Ropero, Jorge M. Nieto, Fernando-Ataúlfo González Fernández, Ana Villegas & Celina Benavente. (2021) Hb Maruchi [α165 (E14) Ala>Pro; HBA1: c.196G>C]: A new thalassemia hemoglobinopathy related to the alpha1 globin gene. Clinical Biochemistry 92, pages 77-81.
Crossref
Giovanna Cardiero, Gennaro Musollino, Maria Grazia Friscia, Rosario Testa, Lucrezia Virruso, Caterina Di Girgenti, Mercedes Caldora, Rosario Colella Bisogno, Carlo Gaudiano, Giuseppe Manco & Giuseppina Lacerra. (2020) Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy. Genes 11:8, pages 870.
Crossref
S. Nair, A. Nadkarni, P. Warang, A. Bhave, K. Ghosh & R. Colah. (2010) Five α globin chain variants identified during screening for haemoglobinopathies. European Journal of Clinical Investigation 40:3, pages 226-232.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 241 265 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
Cristina Passarello, Antonino Giambona, Luciano Prossomariti, Massimiliano Ammirabile, Piero Pucci, Disma Renda, Leonilde Pagano & Aurelio Maggio. (2008) Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie α 2 130 Ala → Pro and Hb Caserta α 2 26 Ala → Thr) in a single HBA2 gene . British Journal of Haematology 143:1, pages 138-142.
Crossref
Anjali A. Sarkar, Chaitali Mukhopadhyay, Sharmila Chandra, Subrata Banerjee, M. K. Das & Uma B Dasgupta. (2005) Co-inheritance of the Hb Sun Prairie mutation with a point mutation at 5'-UTR in the eastern Indian population. British Journal of Haematology 129:2, pages 282-286.
Crossref
John Old. 2004. Genetic Disorders of the Indian Subcontinent. Genetic Disorders of the Indian Subcontinent 245 264 .
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Luigi F. Bernini & Cornelis L. Harteveld. (1998) 2 α-Thalassaemia. Baillière's Clinical Haematology 11:1, pages 53-90.
Crossref
Sara Mach‐Pascual, Regis Darbellay, Pierre‐Antonio Pilotto & Photis Beris. (2009) Investigation of microcytosis: a comprehensive approach. European Journal of Haematology 57:1, pages 54-61.
Crossref
R. DARBELLAY, S. MACH‐PASCUAL, K. ROSE, J. GRAF & PH. BERIS. (2008) Haemoglobin Tunis‐Bizerte: a new a globin 129 Leu–> Pro unstable variant with thalassaemic phenotype . British Journal of Haematology 90:1, pages 71-76.
Crossref
H. Wajcman, C. Vasseur, Y. Blouquit, J. Rosa, D. Labie, A. Najman, O. Reman, M. Leporrier & F. Galacteros. (1993) Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly). American Journal of Hematology 42:4, pages 367-374.
Crossref
G. T. Yuuregir, K. Aksoy, M. A. ÇUuruuk, N. Dikmen, Y.‐J. Fei, E. Baysal & T. H. J. Huisman. (2008) Hb H disease in a Turkish family resulting from the interaction of a deletional α‐thalassaemia‐1 and a newly discovered poly A mutation. British Journal of Haematology 80:4, pages 527-532.
Crossref

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