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Clinica Chimica Acta; International Journal of Clinical Chemistry|December 22, 2015
Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutationFakhri Kallabi, Emna Ellouz, Mouna Tabebi, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetesMouna Tabebi, Wajdi Safi, Rahma Felhi, et al.
Cancers|January 21, 2022
Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in PheochromocytomasMouna Tabebi, Małgorzata Łysiak, Ravi Kumar Dutta, et al.
International Journal of Radiation Biology|March 14, 2017
Oxidative stress and glutathione S-transferase genetic polymorphisms in medical staff professionally exposed to ionizing radiationHajer Doukali, Ghada Ben Salah, Latifa Hamdaoui, et al.
Scientific Reports|January 29, 2025
Modulation of biological activities in adipose derived stem cells by histone deacetylationSallam Abdallah, Mouna Tabebi, Sawsan Qanadilo, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|June 2, 2016
A de-novo large deletion of 2.8 kb produced in the ABCD1 gene causing adrenoleukodystrophy diseaseFakhri Kallabi, Ghada Ben Salah, Amel Ben Chehida, et al.
Biochemical and Biophysical Research Communications|January 21, 2017
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 screeningOlfa Alila-Fersi, Imen Chamkha, Imen Majdoub, et al.
Journal of Diabetes and Its Complications|July 17, 2016
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 mutationMouna Tabebi, Nadia Charfi, Fakhri Kallabi, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|August 11, 2015
Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genesOlfa Fersi Alila, Emna Mkaouar Rebai, Mouna Tabebi, et al.
Biochemical and Biophysical Research Communications|April 2, 2016
Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disordersEmna Mkaouar-Rebai, Rahma Felhi, Mouna Tabebi, et al.
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