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Journal articles

A silent composite hemoglobinopathy characterized by gene sequencing.

A. Zorai** 1 I. Moumni** 2 I. Benmansour 2 D. Chaouachi 2 A. Ghanem 3 S. Abbes 2, 3, * 
* Corresponding author
1 Laboratory of Molecular and Cellular Hematology
LR11IPT07 - Laboratoire d'hématologie moléculaire et cellulaire
2 LR11IPT07 - Laboratoire d'hématologie moléculaire et cellulaire
3 Département de biochimie
Abstract : We report the case of a 35-year-old Tunisian women with a chronic anemia non investigated for a long time. Laboratory analysis using advanced technology of DNA sequencing revealed a compound heterozygote for Hb O Arab and cd 39 beta degrees-thalassemia. It's the first time that such a genotype has been characterized by gene sequencing.
keyword : Chronic anemia Hb O-Arab/ β°-thalassemia association DNA sequencing
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  • HAL Id : pasteur-00821691, version 1
  • PUBMED : 23461145

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A. Zorai**, I. Moumni**, I. Benmansour, D. Chaouachi, A. Ghanem, et al.. A silent composite hemoglobinopathy characterized by gene sequencing.. Archives de l'Institut Pasteur de Tunis, 2011, 88 (1-4), pp.67-70. ⟨pasteur-00821691⟩

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