Researchers track rare muscle disease to pave way for future treatments
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This study follows 150 people with a confirmed genetic diagnosis of primary mitochondrial myopathy, a rare muscle disease. Researchers will track how the disease changes over time using tests like the 6-minute walk and muscle imaging. The goal is to find better ways to measure di…
Sponsor: Cristina Domínguez González • Aim: Knowledge-focused
Last updated May 06, 2026 16:01 UTC