NCT00004769
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +15 more
- Locations
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Not specified
Clinical trial condition
Explore clinical trials studying Muscular Disorders, Atrophic. Study availability and eligibility vary by location and protocol.
NCT00004769
Not specified
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