| 1 |
26993169
| 2016 |
Felhi, R., Mkaouar-Rebai, E., Sfaihi-Ben Mansour, L., Alila-Fersi, O., Tabebi, M., Ben Rhouma, B., Ammar, M., Keskes, L., Hachicha, M., Fakhfakh, F. (2016) Mutational analysis in patients with neuromuscular disorders: Detection of mitochondrial deletion and double mutations in the MT-ATP6 gene Biochemical and Biophysical Research Communications . 473 (1): 61-66. Curator note: patient P1 variants reported in Table2 type out as haplogroup L3f for which 8932T and 8527G are markers. . |