NCT01810965
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +7 more
- Locations
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- CHU Pontchaillou Rennes, France
Clinical trial condition
Hemochromatosis Type 1
Explore clinical trials studying Hemochromatosis Type 1. Study availability and eligibility vary by location and protocol.
1 public trial
0 recruiting studies