NCT03453918
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dysmetabolic Iron Overload Syndrome, Genetic Diseases, Inborn, +14 more
- Locations
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- CHU Clermont-Ferrand Clermont-Ferrand, France
Clinical trial condition
Explore clinical trials studying Genetic Hemochromatosis. Study availability and eligibility vary by location and protocol.
NCT03453918
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