The muscle atrophic phenotype of MuSK myasthenia gravis: Insights from a preclinical rat model
Using a rat model of MuSK myasthenia gravis, this study reveals that MuSK autoimmunity drives selective atrophy of slow-twitch muscle fibers through profound proteome remodeling characterized by disrupted mitochondrial and translational homeostasis, extending beyond mere neuromuscular junction impairment.