Not Yet Recruiting
Implementation of Long-read Sequencing for the Diagnosis of Rare Diseases.
NCT07400913
- Conditions
- Albinism, Amino Acid Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +22 more
- Locations
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- CHU Bordeaux - Hôpital Pellegrin Bordeaux, France