NCT06996756
- Conditions
- Alpha 1-Antitrypsin Deficiency, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, +9 more
- Locations
-
- WCMC Department of Genetic Medicine New York, United States
Clinical trial condition
Explore clinical trials studying Alpha 1-Antitrypsin Deficiency. Study availability and eligibility vary by location and protocol.
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