Rahma Felhi

3PUBLICATIONS
15CO-AUTHORS
Epidemiological methodsMedical biochemistry - lipidsEpigenetics (incl. genome methylation and epigenomics)
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Publications (3)

|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

|Aug 29, 2023
Vitamin B1 deficiency leads to high oxidative stress and mtDNA depletion caused by SLC19A3 mutation in consanguineous family with Leigh syndrome.

Rahma Felhi, Lamia Sfaihi, Majida Charif

|Aug 09, 2022
First description of the MEGDEHL syndrome in the Tunisian population via whole-exome sequencing: Novel nonsense mutation in SERAC1 gene.

Rahma Felhi, Kamel Monastiri, Hayet Ben Hamida

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Frequent Collaborators

2 joint publications

Lamia Sfaihi

2 joint publications

Thouraya Kamoun

1 joint publications

Majida Charif

1 joint publications

Fakher Frikha