Mbarek, I. B., Abroug, S., Omezzine, A., Zellama, D., Achour, A., Harbi, A., & Bouslama, A. (2011). Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria. BioMed Central.

Mbarek, Ibtihel Benhaj, Saoussen Abroug, Asma Omezzine, Dorsaf Zellama, Abdellatif Achour, Abdelaziz Harbi, i Ali Bouslama. Selected AGXT Gene Mutations Analysis Provides a Genetic Diagnosis in 28% of Tunisian Patients With Primary Hyperoxaluria. BioMed Central, 2011.

Mbarek, Ibtihel Benhaj, et al. Selected AGXT Gene Mutations Analysis Provides a Genetic Diagnosis in 28% of Tunisian Patients With Primary Hyperoxaluria. BioMed Central, 2011.