A novel, rapidly progressive ataxia due to a spontaneous Myo5a mutation in mice impairs transport proteins and alters mitochondria
小鼠自发性Myo5a基因突变导致的新型快速进展性共济失调，损害了转运蛋白并改变了线粒体。
期刊:FASEB Journal
影响因子:4.2
doi:10.1096/fj.202402274R
Telenson, Alexander M; Hsieh, Ryan R; Cowen, Gabrielle J; Sode, Eoin P; Kwon, Jason M; Vo, Andy H; Hadhazy, Michele; Page, Patrick G; Rao, Nalini R; Pesce, Lorenzo; Demonbreun, Alexis R; Puckelwartz, Megan J; Savas, Jeffrey N; McNally, Elizabeth M
