Majida Charif
4PUBLICATIONS
16CO-AUTHORS
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Publications (4)
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|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
|Jul 27, 2022
Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy.Majida Charif, Arnaud Chevrollier, Naïg Gueguen
|May 26, 2022
Molecular heterogeneity of β-thalassemia variants in the Eastern region of Morocco.Ihab Belmokhtar, Saida Lhousni, Mounia Elidrissi Errahhali
|Jun 18, 2020
Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy.Majida Charif, Arnaud Chevrollier, Naïg Gueguen
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Frequent Collaborators
3 joint publications
Guy Lenaers
2 joint publications
Arnaud Chevrollier
1 joint publications
Neringa Jurkute
1 joint publications
Leonardo Caporali
1 joint publications
Chiara La Morgia
1 joint publications
Redouane Boulouiz
1 joint publications
Naïg Gueguen
1 joint publications
Fanny Varenne
1 joint publications
Vincent Procaccio
1 joint publications
Pascal Reynier
