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Hemoglobin
international journal for hemoglobin research
Volume 14, 1990 - Issue 6
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Original Article

Hb Hekinan Observed in Three Chinese from Macau; Identification of the Gag→Gat Mutation in the αl-Globin Gene

W. Zhao 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
,
A. Kutlar Department of Cell and Molecular Biology, Laboratory of Protein Chemistry Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
G. P. Tamagnini Hematology Unit, Hospital Central, Macau
,
B. Kuan Hematology Unit, Hospital Central, Macau
&
T. H. J. Huisnan Department of Cell and Molecular Biology, Laboratory of Protein Chemistry Medical College of Georgia, Augusta, GA, 30912-2100, USA
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Pages 627-635 | Received 25 May 1990, Accepted 09 Nov 1990, Published online: 07 Jul 2009

Citations (15)

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Hung-Chang Shih, Mu-Chin Shih, Yu-Chang Chang, Ching-Tien Peng, Tien-Jye Chang & Jan-Gowth Chang. (2007) Hb Hekinan in a Taiwanese Subject: A G→T Substitution at Codon 27 of the α1-Globin Gene Abolishes an HaeIII Site. Hemoglobin 31:4, pages 495-498.
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Lukana Ngiwsara, Chantragan Srisomsap, Pranee Winichagoon, Suthat Fucharoen & Jisnuson Svasti. (2004) Two Cases of Compound Heterozygosity for Hb Hekinan [α27(B8)Glu→Asp (α1)] and α‐Thalassemia in Thailand. Hemoglobin 28:2, pages 145-150.
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Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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M. L. Ribeiro & G. P. Tamagnini. (1997) Hemoglobin Disorders in Macao. Hemoglobin 21:3, pages 271-279.
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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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Jing-Bo Zhao, Lin Zhao, Y-C. Gu & T. H. J. Huisman. (1992) Types of α-Globin Gene Deficiencies in Chinese Newborn Babies in the Guangxi Region, P.R. China. Hemoglobin 16:4, pages 325-328.
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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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Articles from other publishers (8)

Giuseppina Barberio, Massimo Mogni, Massimo Maffei, Giovanni Ivaldi & Livio Caberlotto. (2018) Appropriatezza dei percorsi diagnostici per le emoglobinopatie: il caso Hb HekinanDiagnostic appropriateness of the pathways for hemoglobinopathies: the example of Hb Hekinan. La Rivista Italiana della Medicina di Laboratorio - Italian Journal of Laboratory Medicine 14:1, pages 50-53.
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Hataichanok Srivorakun, Goonnapa Fucharoen, Rawiwan Puangplruk, Napat Kheawon & Supan Fucharoen. (2011) Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α+-thalassemia. European Journal of Haematology 87:1, pages 68-72.
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Kamran Moradkhani, Claude Préhu, John Old, Shirley Henderson, Vera Balamitsa, Hong-Yuan Luo, Man-Chiu Poon, David H. K. Chui, Henri Wajcman & George P. Patrinos. (2008) Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants. Annals of Hematology 88:6, pages 535-543.
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S. Chunpanich, K. Ayukarn, K. Sanchaisuriya, G. Fucharoen & S. Fucharoen. (2004) Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand. Clinical and Laboratory Haematology 26:5, pages 355-358.
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Supan Fucharoen, Yossombat Changtrakun, Thawalwong Ratanasiri, Goonnapa Fucharoen & Kanokwan Sanchaisuriya. (2003) Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family. European Journal of Haematology 70:5, pages 304-309.
Crossref
T. P. Molchanova, D. D. Pobedimskaya & T. H. J. Huisman. (1994) The differences in quantities of α2-and α1-globin gene variants in heterozygotes. British Journal of Haematology 88:2, pages 300-306.
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Titus H.J. Huisman. (1993) 1 The structure and function of normal and abnormal haemoglobins. Baillière's Clinical Haematology 6:1, pages 1-30.
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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.
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