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Hemoglobin
international journal for hemoglobin research
Volume 27, 2003 - Issue 2
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Original

Co‐existence of the Codon 16 (–C) (β0) and Codon 10 (C→A) (β+) Mutations on the Same β‐Globin Gene

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Pages 133-135 | Received 23 Dec 2002, Accepted 20 Jan 2003, Published online: 07 Jul 2009

References

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  • Krugluger W., Hopmeier P. Identification of a compound β‐thalassemia homozygosity [codon 10 (GCC→GCA) and codon 16 (−C)] in an Afghan family. Hemoglobin 2002; 26(3)317–320
  • Pawar A. R., Colah R. B., Mohanty D. A novel β+ thalassemia mutation (codon 10 GCC→GCA) and a rare transcriptional mutation (−28 A→G) in Indians. Blood 1997; 89: 3888–3889
  • Huisman T. H.J., Carver M. F.H., Efremov G. D. A Syllabus of Human Hemoglobin Variants2nd. The Sickle Cell Anemia Foundation, Augusta 1998, (http://globin.cse.psu.edu)

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