F. H. Kacem

A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations

M. Abid, A. Tlili, F. Fakhfakh, 2022 .

Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian population

A. Odermatt, L. Keskes, T. Kammoun, 2022, The Journal of Steroid Biochemistry and Molecular Biology.