Olfa-Alila Fersi
4PUBLICATIONS
13CO-AUTHORS
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Publications (4)
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|Mar 12, 2024
Expanding the genetic and phenotypic spectrum of TRAPPC9 and MID2-related neurodevelopmental disabilities: report of two novel mutations, 3D-modelling, and molecular docking studies.Marwa Kharrat, Chahnez Triki, Abir Ben Isaa
|Feb 16, 2024
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.Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi
|Sep 01, 2023
A novel homozygous PIGO mutation associated with severe infantile epileptic encephalopathy, profound developmental delay and psychomotor retardation: structural and 3D modelling investigations and genotype-phenotype correlation.Ameni Aguech, Lamia Sfaihi, Olfa Alila-Fersi
|Mar 04, 2020
Mutations in GAA Gene in Tunisian Families with Infantile Onset Pompe Disease: Novel Mutation and Structural Modeling Investigations.Olfa Alila-Fersi, Hajer Aloulou, Ines Werteni
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Frequent Collaborators
2 joint publications
Lamia Sfaihi
2 joint publications
Abdelaziz Tlili
2 joint publications
Thouraya Kammoun
2 joint publications
Faiza Fakhfakh
1 joint publications
Ameni Aguech
1 joint publications
Roeya Kolsi
1 joint publications
Ahmed Fendri
1 joint publications
Marwa Maalej
1 joint publications
Boudour Khabou
1 joint publications
Marwa Ammar
