Publications by authors named "I Mosbahi"

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Rare hemoglobin variants in Tunisian population.
A Zorai, I Moumni, I Mosbahi, K Douzi, D Chaouachi

Int J Lab Hematol· April 2015

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A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
Imen Moumni, Amine Zorai, Sonia Mahjoub, Ikbel Mosbahi, Dorra Chaouechi

Hemoglobin· December 2014

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Three new mutations account for the prevalence of glucose 6 phosphate deshydrogenase (G6PD) deficiency in Tunisia.
B Bendaoud, I Hosni, I Mosbahi, R Hafsia, C Prehu

Pathol Biol (Paris)· April 2013

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Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation.
Imen Moumni, Amine Zorai, Bechir Ben Daoued, Ikbel Mosbahi, Souheil Omar

Hemoglobin· May 2007

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