NCT04658381
- Conditions
- Albinism, Amino Acid Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +12 more
- Locations
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- Hôpital Fondation A. de Rothschuld Paris, France
Clinical trial condition
Explore clinical trials studying Skin Diseases, Genetic. Study availability and eligibility vary by location and protocol.
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