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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
French Observatory for Patients with Type 3 GlycogenosisCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, disorder of glycogen metabolism, glycogen storage disease III, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, metabolic diseaseRecruitingNot stated2024-09-27NCT06616545