| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 27155156 | 2016 | Ammar, M., Tabebi, M., Sfaihi, L., Alila-Fersi, O., Maalej, M., Felhi, R., Chabchoub, I., Keskes, L., Hachicha, M., Fakhfakh, F., Mkaouar-Rebai, E. (2016) Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene Biochemical and Biophysical Research Communications . 474 (4): 702-708 . |