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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Natural History Study for Patients With Angelman SyndromeAbnormalities, Multiple, Angelman syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Imprinting Disorders, central nervous system disorder, chromosomal disorder, hereditary disease, movement disorder, nervous system disorderRecruitingNot stated2025-05-20NCT06229769

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Research sitesCityCountryLinked trials
CHR Citadelle LiègeLiègeBelgium2