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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 3
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Short Communication

Nondeletional Hb Queens Park [α32(B13)Met→Lys]/Hb H (β4) Disease

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Pages 293-298 | Received 10 Oct 2011, Accepted 22 Dec 2011, Published online: 02 Mar 2012

REFERENCES

  • Winichagoon P, Fucharoen S, Wasi P. The molecular basis of α-thalassemia in Thailand. Southeast Asian J Trop Med Public Health. 1992;23(Suppl. 2):7–13.
  • Fucharoen S, Viprakasit V. Hb H disease: clinical course and disease modifiers. Hematology Am Soc Hematol Educ Program. 2009:26–34.
  • Singsanan S, Fucharoen G, Savongsy O, Sanchaisuriya K, Fucharoen S. Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations. Ann Hematol. 2007;86(9):665–669.
  • Pichanun D, Munkongdee T, Klamchuen S, Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand. Hemoglobin. 2010;34(6):582–586.
  • Laosombat V, Fucharoen S, Wiriyasateinkul A. Interaction of the α2 polyadenylation signal mutation (AATAAA→AATA– –) and α0-thalassemia (– –SEA), resulting in Hb H disease in a Thai patient. Hemoglobin. 2001;25(4):383–389.
  • Viprakasit V, Chinchang W, Glomglao W, Tanphaichitr VS. 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. 2005;29(3):235–240.
  • Moradkhani K, Mazurier E, Giordano PC, Wajcman H, Prehu C. An α0-thalassemia-like mutation: Hb Suan-Dok [α109(G16)Leu→Arg] carried by a recombinant –α3.7 gene. Hemoglobin. 2008;32(4):419–424.
  • Sura T, Trachoo O, Viprakasit V, Hemoglobin H disease induced by the common SEA deletion and the rare Hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method. Ann Hematol. 2007;86(9):659–663.
  • Harteveld CL, Beijer C, van Delft P, Zanardini R, Bernini LF, Giordano PC. α-Thalassaemia as a result of a novel splice donor site mutation of the α1-globin gene. Br J Haematol. 2000;110(3):694–698.
  • Viprakasit V, Tanphaichitr VS, Veerakul G, Co-inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α0 thalassemia associated with transfusion-dependent Hb H disease. Am J Hematol. 2004;75(3):157–163.
  • Chong SS, Boehm CD, Cutting GR, Higgs DR. Simplified multiplex-PCR diagnosis of common Southeast Asian deletional determinants of α-thalassemia. Clin Chem. 2000;46(10):1692–1695.
  • Chong SS, Boehm CD, Higgs DR, Cutting GR. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood. 2000;95(1):360–362.
  • Fucharoen S, Fucharoen G, Fukumaki Y. Simple non-radioactive method for detecting Haemoglobin Constant Spring gene. Lancet. 1990;335(8704):1527.
  • Fucharoen S, Sanchaisuriya K, Fucharoen G, Panyasai S, Devenish R, Luy L. Interaction of Hemoglobin E and several forms of α-thalassemia in Cambodian families. Haematologica. 2003;88(10):1092–1098.
  • Phylipsen M, Prior JF, Lim E, Two new α1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [α28(B9)Ala→Val] and Hb Queens Park (HBA1:c.98T>A) [α32(B13)Met→Lys]. Hemoglobin. 2010;34(2):123–126.
  • Turbpaiboon C, Wilairat P. α-Hemoglobin stabilizing protein: molecular function and clinical correlation. Front Biosci. 2010;15:1–11.
  • Wajcman H, Traeger-Synodinos J, Papassotiriou I, Unstable and thalassemic α chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia. Hemoglobin. 2008;32(4):327–349.
  • Harteveld CL, Vervloet M, Zweegman S, Hb Amsterdam [α32(B13)Met→Ile (α2)]: a new unstable variant associated with an α-thalassemia phenotype and a new African polymorphism. Hemoglobin. 2005;29(4):257–262.
  • Giordano PC, Cnossen MH, Joosten AM, Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel α2 gene mutations associated with mild α-thalassemia found in the same family after newborn screening. Hemoglobin. 2010;34(4):354–365.
  • Albitar M, Cash FE, Peschle C, Liebhaber SA. Developmental switch in the relative expression of the α1- and α2-globin genes in humans and in transgenic mice. Blood. 1992;79(9):2471–2474.

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