Index | PMID | Date | Reference |
---|---|---|---|
1 | 20525945 | 2010 | Mkaouar-Rebai, E., Ellouze, E., Chamkha, I., Kammoun, F., Triki, C., Fakhfakh, F. (2010) Molecular-clinical correlation in a family with a novel heteroplasmic Leigh Syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene Journal of Child Neurology . 26 (1): 12-20 . |
2 | 23301511 | 2013 | Mkaouar-Rebai, E., Chamkha, I., Mezghani, N., Ben Ayed, I., Fakhfakh, F. (2013) Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: an overview study Mitochondrial DNA . 24 (3): 163-178 . |
3 | 29253894 | 2017 | Wei, W., Gomez-Duran, A., Hudson, G., Chinnery, P. F. (2017) Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations PLoS Genetics . 13 (12): e1007126 . |