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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 4
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Original

INTERACTION OF THE α2 POLYADENYLATION SIGNAL MUTATION (AATAAA → AATA– –) AND α0-THALASSEMIA (– –SEA), RESULTING IN Hb H DISEASE IN A THAI PATIENT

Vichai Laosombat Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkla, 90110, Thailand
,
Supan Fucharoen Department of Clinical Chemistry, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand
&
Aranya Wiriyasateinkul Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkla, 90110, Thailand
Pages 383-389 | Received 01 Jun 2001, Accepted 16 Jul 2001, Published online: 07 Jul 2009

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Pacharapan Surapolchai, Nongnuch Sirachainan, Chi-Chiu So, Suradej Hongeng, Samart Pakakasama, Usanarat Anurathapan & Ampaiwan Chuansumrit. (2016) Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses. Hemoglobin 40:1, pages 70-73.
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Prashant Deshpande, Neelagandan Kamalanathan, Eswari Sampath, Biju George, Ramachandran V. Shaji & Eunice S. Edison. (2015) Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA– –) in an Indian Population. Hemoglobin 39:6, pages 415-418.
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Sona B. Nair, Anita H. Nadkarni, Kanjaksha Ghosh & Roshan B. Colah. (2013) Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A TIndian (AATAAA>AATA– –) Mutation in Four Indian Families. Hemoglobin 37:3, pages 277-284.
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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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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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Vip Viprakasit, Worrawut Chinchang, Waraporn Glomglao & Voravarn S Tanphaichitr. (2005) 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. Hemoglobin 29:3, pages 235-240.
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Articles from other publishers (8)

Wittaya Jomoui & Wanicha Tepakhan. (2021) Characterization and identification of Prachinburi β 0 ‐thalassemia: A novel‐60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state . International Journal of Laboratory Hematology 43:4.
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V. Viprakasit. (2015) α−thalassaemia: a genotype-phenotype correlation and management. ISBT Science Series 10:S1, pages 295-304.
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Vichai Laosombat, Vip Viprakasit, Thirachit Chotsampancharoen, Malai Wongchanchailert, Sudarat Khodchawan, Worawut Chinchang & Benjamas Sattayasevana. (2009) Clinical features and molecular analysis in Thai patients with HbH disease. Annals of Hematology 88:12, pages 1185-1192.
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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 .
Shirley Henderson, Mary Chapple, Michele Rugless, Chris Fisher, Sally Kinsey & John Old. (2006) Haemoglobin H hydrops fetalis syndrome associated with homozygosity for the ?2-globin gene polyadenylation signal mutation AATAAA?AATA?�?. British Journal of Haematology 135:5, pages 743-745.
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Supap Boonsa, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Surapon Wiangnon, Arunee Jetsrisuparb & Supan Fucharoen. (2004) The Diverse Molecular Basis and Hematological Features of Hb H and AEBart’s Diseases in Northeast Thailand. Acta Haematologica 111:3, pages 149-154.
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Joanne Traeger-Synodinos, Ioannis Papassotiriou, Markissia Karagiorga, Evangelos Premetis, Emmanuel Kanavakis & Alexandra Stamoulakatou. (2002) Unusual phenotypic observations associated with a rare HbH disease genotype (- - Med /α TSaudi α): implications for clinical management . British Journal of Haematology 119:1, pages 265-267.
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