| 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 . |