Service interruption on Monday 11 July from 12:30 to 13:00: all the sites of the CCSD (HAL, Epiciences, SciencesConf, AureHAL) will be inaccessible (network hardware connection).
Skip to Main content Skip to Navigation
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, * 
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.
Complete list of metadata

Cited literature [17 references]  Display  Hide  Download

https://hal-riip.archives-ouvertes.fr/pasteur-00821691
Contributor : Institut Pasteur Tunis Connect in order to contact the contributor
Submitted on : Saturday, May 11, 2013 - 9:20:17 PM
Last modification on : Wednesday, October 28, 2020 - 9:52:03 AM
Long-term archiving on: : Monday, August 12, 2013 - 5:20:07 AM

File

A.Zorai_et_coll.pdf
Explicit agreement for this submission

Identifiers

  • HAL Id : pasteur-00821691, version 1
  • PUBMED : 23461145

Collections

Citation

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⟩

Share

Metrics

Record views

33

Files downloads

389