RECESSIVE HEREDITARY DISORDER (AUTOSOMAL)

Clinical trials for RECESSIVE HEREDITARY DISORDER (AUTOSOMAL) explained in plain language.

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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 …

Matched conditions: RECESSIVE HEREDITARY DISORDER (AUTOSOMAL)

Sponsor: Clinic for Special Children • Aim: Knowledge-focused

Last updated Jun 27, 2026 14:01 UTC

RECESSIVE HEREDITARY DISORDER (AUTOSOMAL)

Get alerted when new RECESSIVE HEREDITARY DISORDER (AUTOSOMAL) trials appear

Global study tracks rare muscle disease to pave way for future treatments