Thouraya Kammoun

Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low‐GGT intrahepatic cholestasis: Genetic diagnosis and genotype–phenotype correlation assessment

F. Fakhfakh, B. Khemakhem, A. B. Chehida, 2023, Annals of human genetics.

Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity.

A. Tlili, F. Fakhfakh, R. Felhi, 2024, Metabolic brain disease.