论文信息 - Mutational analysis in patients with neuromuscular disorders: Detection of mitochondrial deletion and double mutations in the MT-ATP6 gene. - 字舞流文

Mutational analysis in patients with neuromuscular disorders: Detection of mitochondrial deletion and double mutations in the MT-ATP6 gene.

F. Fakhfakh | M. Hachicha | L. Keskes | R. Felhi | Mouna Tabebi | E. Mkaouar-Rebai | Olfa Alila-Fersi | Marwa Ammar | Lamia Sfaihi-Ben Mansour | Bochra Ben Rhouma