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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
The Effect of Monoallelic Variants in the ALPL Gene on the Natural Course of Hypophosphatasia in RussiaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, hypophosphatasia, inborn errors of metabolism, inborn metal metabolism disorder, metabolic diseaseRecruitingNot stated2026-09-28NCT07390240

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AstraZeneca806

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