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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 5
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Original Article

Molecular Scanning of β-Thalassemia in the Southern Region of Central Java, Indonesia; a Step Towards a Local Prevention Program

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Pages 330-333 | Received 21 Dec 2014, Accepted 15 Mar 2015, Published online: 03 Aug 2015

References

  • Galanello R, Origa R. β-Thalassemia. Orphanet J Rare Dis. 2010;5:11. doi: 10.1186/1750-1172-5-11
  • Weatherall, DJ. Thalassemia as a global health problem: Recent progress toward its control in the developing countries. Ann N Y Acad Sci. 2010;1202:17–23
  • Sofro AS. Molecular pathology of β-thalassemia in Indonesia. Southeast Asian J Trop Med Public Health. 1995;26(Suppl 1):221–224
  • Thalassaemia prevention (Health Technology Assessment Study 2009). Medical Service Bureau. Jakarta, INA: Ministry of Health, Republic of Indonesia, 2010. (http://www.academia.edu/9564064/Health_Tecnology_Assessment_Indonesia)
  • Giordano P, Harteveld C, Bakker E. Genetic epidemiology and preventive healthcare in multiethnic societies: The hemoglobinopathies. Int J Environ Res Public Health. 2014;11(6):6136–6146
  • Setianingsih I, Williamson R, Marzuki S, et al. Molecular basis of β-thalassemia in Indonesia: Application to prenatal diagnosis. Mol Diagn. 1998;3(1):11–19
  • Tamam M, Hadisaputro S, Sutaryo S, et al. The relationship between type of globin gene mutation and clinical manifestations in patients with thalassaemia. Jurnal Kedokteran Brawijaya (JKB). 2010;26(1):48–52. (http://jkb.ub.ac.id/index.php/jkb/article/view/126 )
  • Hernanda PY, Tursilowati L, Arkesteijn SG, et al. Towards a prevention program for β-thalassemia. The molecular spectrum in East Java, Indonesia. Hemoglobin. 2012;36(1):1–6
  • van Delft P, Lenters E, Bakker-Verweij M, et al. Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations. Int J Lab Hematol. 2009;31(5):484–495
  • Pramoonjago P, Harahap A, Taufani RA, et al. Rapid screening for the most common β thalassaemia mutations in south east Asia by PCR based restriction fragment length polymorphism analysis (PCR-RFLP). J Med Genet, 1999;36(12):927–938
  • Chan OT, Westover L, Dietz JL, et al. Comprehensive and efficient HBB mutation analysis for detection of β-hemoglobinopathies in a pan-ethnic population. Am J Clin Pathol. 2010;133(5):700–707
  • Hapsari AT, Rujito L. Diagnostic test of blood index and molecular identitication of β-thalassemia carrier in blood donors of Banyumas area. Jurnal Kedokteran Brawijaya (JKB). 2015;281(1):233–237. (http://jkb.ub.ac.id/index/php/jkb/article/view/595)
  • Lie-Injo LE, Cai SP, Wahidijat I, et al. β-Thalassemia mutations in Indonesia and their linkage to β haplotypes. Am J Hum Genet. 1989;45(6):971–975
  • Olivieri NF, Pakbaz Z, Vichinsky E. Hb E/β-thalassemia: Basis of marked clinical diversity. Hematol Oncol Clin North Am. 2010;24(6):1055–1070
  • Yin A, Li B, Luo M, et al. The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China. PLoS ONE, 2014;9(2):e89855. doi: 10.1371/journal.pone.0089855
  • Fucharoen S,Winichagoon P. Haemoglobinopathies in Southeast Asia. Indian J Med Res. 2011;134(4):498–506
  • Srivorakun H, Singha K, Fucharoen G, et al. A large cohort of hemoglobin variants in Thailand: Molecular epidemiological study and diagnostic consideration. PLoS ONE. 2014;9(9):e108365. doi: 10.1371/journal.pone.0108365
  • Gonzales-Redondo J, Stoming TA, Kutlar F, et al. Severe Hb S-β0-thalassaemia with a T→C substitution in the donor splice site of the first intron of the β-globin gene. Br J Haematol. 1989;71(1):113–117
  • Weatherall DJ, Clegg JB. The Thalassaemia Syndromes, 4th ed. Oxford, UK: Blackwell Science, 2001
  • Ohba Y, Hattori Y, Harano T, et al. β-Thalassemia mutations in Japanese and Koreans. Hemoglobin. 1997;21(2):191–200
  • Giardine B, Borg J, Viennas E, et al. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations. Nucleic Acids Res. 2014;42(Database Issue):D1063–D1069. (http://globin.cse.psu.edu)
  • Fucharoen G, Fuchareon S, Jetsrisuparb A, Fukumaki Y. Eight-base deletion in exon 3 of the β-globin gene produced a novel variant (β Khon Kaen) with an inclusion body β-thalassemia trait. Blood. 1991;78(2):537–539

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