Identification of a muscle-specific isoform of VMA21 as a potent actor in X-linked myopathy with excessive autophagy pathogenesis
鉴定出VMA21的肌肉特异性亚型是X连锁肌病伴过度自噬发病机制中的重要因素
期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddad164
Cocchiararo, Ilaria; Cattaneo, Olivia; Rajendran, Jayasimman; Chabry, Florent; Cornut, Mélanie; Soldati, Hadrien; Bigot, Anne; Mamchaoui, Kamel; Gibertini, Sara; Bouche, Axelle; Ham, Daniel J; Laumonier, Thomas; Prola, Alexandre; Castets, Perrine
