NCT01406977
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hypophosphatasia, +4 more
- Locations
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- Mereo BioPharma 3 Ltd Investigative Site Würzburg, Germany
Clinical trial condition
Explore clinical trials studying Hypophosphatasia. Study availability and eligibility vary by location and protocol.
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