NCT01676688
- Conditions
- Alpha 1-Antitrypsin Deficiency, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, +9 more
- Locations
-
Not specified
Clinical trial condition
Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.
NCT01676688
Not specified
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