Olfa Alila‐Fersi

Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation

Mouna Tabebi, Nadia Charfi, Fakhri Kallabi et al. · Journal of Diabetes and its Complications · 2016 · 18 citations

Mendelian Disorder, Ophthalmology, Genetic Disorder +10

Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochondrial genome screening

Olfa Alila‐Fersi, Imen Chamkha, I. Majdoub et al. · Biochemical and Biophysical Research Communications · 2017 · 15 citations

Molecular Physiology, Mendelian Disorder, Mitochondrial Function +10

Mutational analysis in patients with neuromuscular disorders: Detection of mitochondrial deletion and double mutations in the MT-ATP6 gene

Rahma Felhi, Emna Mkaouar‐Rebai, L. Sfaihi et al. · Biochemical and Biophysical Research Communications · 2016 · 11 citations

Mitochondrial Myopathy, Mt-atp6 Gene, Mutational Analysis +9

First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy

Olfa Alila‐Fersi, Mouna Tabebi, Marwa Maalej et al. · Biochemical and Biophysical Research Communications · 2018 · 10 citations