Scientists probe muscle secrets in rare disease
NCT ID NCT06096441
Summary
This study aimed to better understand the muscle changes in people with facioscapulohumeral muscular dystrophy (FSHD), a genetic muscle-wasting disease. Researchers planned to analyze small muscle samples and MRI scans from participants to identify biological markers linked to the disease. The goal was to gather information to help design future treatment trials, but the study was terminated early.
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Contacts and locations
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Locations
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The Abigail Wexner Research Institute at Nationwide Children's Hospital
Columbus, Ohio, 43205, United States
Conditions
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