NCT01810965
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +7 more
- Locations
-
- CHU Pontchaillou Rennes, France
Clinical trial condition
Explore clinical trials studying Metal Metabolism, Inborn Errors. Study availability and eligibility vary by location and protocol.
NCT01810965
NCT02007746
NCT03867526
NCT00195936
NCT02763215
NCT00811785
NCT03596554
NCT04546022
Not specified
NCT03299829
NCT01472874