NCT01422200
- Conditions
- Central Nervous System Diseases, Congenital Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +22 more
- Locations
-
Not specified
Clinical trial condition
Explore clinical trials studying Spinal Muscular Atrophy. Study availability and eligibility vary by location and protocol.
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Not specified
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