Index | PMID | Date | Reference |
---|---|---|---|
1 | 27422531 | 2017 | Tabebi, M., Charfi, N., Kallabi, F., Alila-Fersi, O., Ben Mahmoud, A., Tlili, A., Keskes-Ammar, L., Kamoun, H., Abid, M., Mnif, M., Fakhfakh, F. (2017) 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 Journal of Diabetes and its Complications . 31 (1): 253-259 . |
2 | 28890306 | 2017 | Finsterer, J., Zarrouk-Mahjoub, S. (2017) Variants m.13276G>A in the MT-ND5 and m.8241T>G in the MT-CO2 gene are not responsible for maternally inherited diabetes and deafness Journal of Diabetes and its Complications . 31 (11): 1638 . |