검색결과 : 4건
| No. | Article |
|---|---|
| 1 |
Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome Maalej M, Kammoun T, Alila-Fersi O, Kharrat M, Ammar M, Felhi R, Mkaouar-Rebai E, Keskes L, Hachicha M, Fakhfakh F Biochemical and Biophysical Research Communications, 497(4), 1043, 2018 |
| 2 |
A novel MT-CO1 m.6498C > A variation associated with the m.7444G > A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing Mkaouar-Rebai E, Chamkha I, Kammoun T, Alila-Fersi O, Aloulou H, Hachicha M, Fakhfakh F Biochemical and Biophysical Research Communications, 430(2), 585, 2013 |
| 3 |
A novel m.3395A > G missense mutation in the mitochondrial ND1 gene associated with the new tRNA(Ile) m.4316A > G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss Chamkha I, Mkaouar-Rebai E, Aloulou H, Chabchoub I, Kifagi C, Fendri-Kriaa N, Kammoun T, Hachicha M, Fakhfakh F Biochemical and Biophysical Research Communications, 404(1), 504, 2011 |
| 4 |
A Tunisian patient with Pearson syndrome harboring the 4.977 kb common deletion associated to two novel large-scale mitochondrial deletions Ben Ayed I, Chamkha I, Mkaouar-Rebai E, Kammoun T, Mezghani N, Chabchoub I, Aloulou H, Hachicha M, Fakhfakh F Biochemical and Biophysical Research Communications, 411(2), 381, 2011 |