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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 5
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Original Article

Hb Midnapore [β53(D4)Ala→Val; HBB: c.161C>T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G>C) (HBB: c.92+5G>C) Found in a Bengali Indian Family

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Pages 300-303 | Received 26 Jun 2016, Accepted 12 Sep 2016, Published online: 08 Nov 2016

References

  • Sharma S, Sharma G, Chandra J, et al. Hemoglobin Agenogi ? A rare abnormal β globin chain variant. Indian J Pathol Microbiol. 2016;59(1):99–101.
  • Kohne E. Hemoglobinopathies: clinical manifestations, diagnosis, and treatment. Dtsch Arztebl Int. 2011;108(31-32):532–540.
  • Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537–D541. (http://globin.cse.psu.edu).
  • Agarwal S, Hattori Y, Gupta UR, Agarwal SS. A novel Indian β-thalassemia mutation: Hb Lucknow [β8(A5)Lys→Arg]. Hemoglobin. 1999;23(3):263–265.
  • Rao S, Kar R, Gupta SK, et al. Spectrum of haemoglobinopathies diagnosed by cation exchange-HPLC; modulating effects of nutritional deficiency anaemias from north India. Indian J Med Res. 2010;132:513–519.
  • Old J, Harteveld CL, Traeger-Synodinos J, et al. Prevention of Thalassaemias and Other Haemoglobin Disorders, Volume 2: Laboratory Protocols. Nicosia, Cyprus: Thalassaemia International Federation Publications; 2004.
  • Papassotiriou I, Traeger-Synodinos J, Promé D, et al. Association of unstable hemoglobin variants and heterozygous β-thalassemia: example of a new variant Hb Acharnes or [β53(D4)Ala→Thr]. Am J Hematol. 1999;62(3):186–192.
  • Gaudry CL Jr, Pitel PA, Jue DL, et al. Hb Jacksonville [α2β254(D5)Val→Asp]: a new unstable variant found in a patient with hemolytic anemia. Hemoglobin. 1990;14(6):653–659.
  • Williams JP, Scrivens JH, Green BN, et al. Hb Leeds [β56(D7)Gly→Cys]: a new hemoglobin that aggravates anemia in a child with β0-thalassemia trait. Hemoglobin. 2007;31(3):367–373.
  • Sciarratta GV, Ivaldi G. Hb Matera [β55(D6)Met→Lys]: a new unstable hemoglobin variant in an Italian family. Hemoglobin. 1990;14(1):79–185.
  • Divoky V, Bissé E, Wilson JB, et al. Heterozygosity for the IVS-I-5 (G→C) mutation with a G→A change at codon 18 (Val→Met; Hb Baden) in cis and a T→G mutation at codon 126 (Val→Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. Biochim Biophys Acta. 1992;10(1180):173–179.

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