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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of the Pathophysiology of RNU4ATAC and RTTN Associated SyndromesCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Lowry-Wood syndrome, Roifman syndrome, hereditary disease, microcephalic osteodysplastic primordial dwarfism type I, microcephalic osteodysplastic primordial dwarfism types I and IIIRecruitingNot applicable2024-10-09NCT06111950