NCT03654794
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +6 more
- Locations
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- CHU de Rennes Rennes, France
Clinical trial condition
Explore clinical trials studying Hemochromatosis. Study availability and eligibility vary by location and protocol.
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