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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 4
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Original Article

Identification of a Novel β0Thalassemia Mutation, Codons 80181 (−C), in an Iranian Family

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Pages 319-321 | Received 28 Mar 2000, Accepted 27 Apr 2000, Published online: 07 Jul 2009

References

  • Baysal E., Carver M. F.H. The β‐ and δ‐thalassemia repository (eighth edition). Hemoglobin 1995; 19: 213–236
  • Newton C. R., Graham A., Heptinstall L. E., Powell S. J., Summers C., Kalshekar N., Smith J. C., Markham A. E. Analysis of any point mutation in DNA: the amplification refractory mutation system (ARMS). Nucleic Acids Res. 1989; 17: 2503–2516
  • Old J. M., Varawalla N. Y., Weatherall D. J. Rapid detection and prenatal diagnosis of β‐thalassaemia: studies in Indian and Cypriot populations in the UK. The Lancet 1990; 336: 834–837
  • Losekoot M., Fodde R., Harteveld C. L., Heeren H. V., Giordano P. C., Went L. N., Bernini L. F. Homozygous β+ thalassemia owing to a mutation in the cleavage‐polyadenyl‐ation sequence of the human β globin gene. J. Med. Genet. 1991; 28: 252–255
  • Ghanem N., Girodon E., Vidaud M., Martin J., Fanen P., Plassa F., Goossens M. A comprehensive scanning method for rapid detection of β‐globin gene mutations and polymorphisms. Hum. Mut. 1992; 1: 229–239

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