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Author/Creator Boudriga, Imen

1. Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome. (4th March 2017)

Authors:
Haddad, Faten; Trabelsi, Nawel; Chaouch, Leila; Darragi, Imen; Oueslati, Meriem; Boudriga, Imen; Chaouachi, Dorra; El-Borgi, Wijdene; Hafsia, Raouf; Abbes, Salem; Ouragini, Houyem
Journal:
Hemoglobin
Issue:
Volume 41:Number 2(2017)
Page Start:
147
Record Type:
Journal Article
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2. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)0-Thalassemia among Tunisian family. (March 2023)

Authors:
Kalai, Miniar; Moumni, Imen; Ouragini, Houyem; Ben Fraj, Ilhem; Mellouli, Fethi; Ouederni, Monia; Chaouachi, Dorra; Boudriga, Imen; Menif, Samia
Journal:
Annals of clinical biochemistry
Issue:
Volume 60:Number 2(2023)
Page Start:
81
Record Type:
Journal Article
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