Global study tracks rare muscle disease to pave way for future treatments
Knowledge-focused
Recruiting now
This study follows children and adults worldwide who have a rare genetic muscle disease called TNNT1 myopathy. Researchers aim to document how the disease progresses over time, including survival and motor milestones. The goal is to identify reliable measures that can be used in …
Sponsor: Clinic for Special Children • Aim: Knowledge-focused
Last updated Jun 27, 2026 14:01 UTC