NCT02835079
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
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Not specified
Clinical trial condition
Explore clinical trials studying Duchenne Muscular Dystrophy. Study availability and eligibility vary by location and protocol.
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