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Hemoglobin
international journal for hemoglobin research
Volume 29, 2005 - Issue 3
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Short Communication

A Rare Association of α0-Thalassemia (– –SEA) and an Initiation Codon Mutation (ATG→A-G) of the α2 Gene Causes Hb H Disease in Thailand

Vip Viprakasit Department of Paediatrics, Siriraj Thalassaemia Research Program and the World Health Organization (WHO) Collaborating Center for the Control of Haemoglobinopathies, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, ThailandCorrespondence[email protected]
, D.Phil. (Oxon) , M.D.,
Worrawut Chinchang Department of Paediatrics, Siriraj Thalassaemia Research Program and the World Health Organization (WHO) Collaborating Center for the Control of Haemoglobinopathies, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand
,
Waraporn Glomglao Department of Paediatrics, Siriraj Thalassaemia Research Program and the World Health Organization (WHO) Collaborating Center for the Control of Haemoglobinopathies, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand
&
Voravarn S Tanphaichitr Department of Paediatrics, Siriraj Thalassaemia Research Program and the World Health Organization (WHO) Collaborating Center for the Control of Haemoglobinopathies, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand
Pages 235-240 | Received 21 Mar 2004, Accepted 11 Apr 2005, Published online: 07 Jul 2009

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Shiqiang Luo, Xingyuan Chen, Lizhu Chen, Qingyan Zhong, Qiuhua Wang, Zehui Xu, Jun Huang, Tizhen Yan & Ning Tang. (2020) Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease. Expert Review of Hematology 13:9, pages 1027-1033.
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Ya-Li Lei, Hong Sui, Yu-Juan Liu, Jun-Jun Pan, Yan-Hui Liu & Ji-Wu Lou. (2019) Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C). Hemoglobin 43:4-5, pages 241-244.
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John S. Waye, Barry Eng, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura & Lynda Walker. (2016) Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A). Hemoglobin 40:5, pages 369-370.
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Suravee Sroymora, Sumalee Jindadamrongwech, Punnee Butthep & Suporn Chuncharunee. (2012) Nondeletional Hb Queens Park [α32(B13)Met→Lys]/Hb H (β4) Disease. Hemoglobin 36:3, pages 293-298.
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Articles from other publishers (2)

Divashini Vijian, Wan Suriana Wan Ab Rahman, Kannan Thirumulu Ponnuraj & Zefarina Zulkafli. (2022) Clinical and Haematological Parameters of Commonly Reported Non-deletional α-thalassaemia Mutations in Southeast Asia: A Review. Malaysian Journal of Medicine and Health Sciences 18:5, pages 190-199.
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Shiqiang Luo, Xingyuan Chen, Dingyuan Zeng, Ning Tang, Dejian Yuan, Qingyan Zhong, Aiping Mao, Ruofan Xu & Tizhen Yan. (2021) The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype–genotype correlation. Journal of Human Genetics 67:4, pages 183-195.
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