A novel mutation in FDX2 provides insights into the pathogenesis of MEOAL mitochondrial neuromuscular disease
FDX2基因中的一种新突变为MEOAL线粒体神经肌肉疾病的发病机制提供了新的见解
期刊:Cell Death & Disease
影响因子:9.6
doi:10.1038/s41419-025-08323-3
Doni, Davide; Grifagni, Deborah; Cavion, Federica; Buchignani, Bianca; Battini, Roberta; Baschiera, Elisa; Desbats, Maria Andrea; Pasquariello, Rosa; Covello, Giuseppina; De Pascale, Eva; Boarolo, Alice; Cestonaro, Ilaria; Badocco, Denis; Pastore, Paolo; Sartori, Geppo; Stehling, Oliver; Lill, Roland; Santorelli, Filippo M; Salviati, Leonardo; Ciofi-Baffoni, Simone; Costantini, Paola
