500-Patient study aims to unlock secrets of rare nerve and muscle diseases
NCT ID NCT04417023
First seen Jan 07, 2026 · Last updated May 13, 2026 · Updated 21 times
Summary
This study collects blood, tissue, and imaging data from 500 adults with neuromuscular diseases (like ALS, muscular dystrophy, or neuropathy). The goal is to find genetic markers and better ways to diagnose these rare conditions quickly. Researchers hope this knowledge will lead to future treatments.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Ottawa Hospital Research Institute
Ottawa, Ontario, K1Y4E9, Canada
Conditions
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