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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Renal and Vascular Phenotypic Characterization of Patients With Enamel Renal Syndrome Due to a Pathogenic Variant of the FAM20A Gene and Pathophysiological Study of Ectopic Calcificationsamelogenesis imperfecta type 1GNot yet recruitingNot applicable2025-12-16NCT07285421

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Research sitesCityCountryLinked trials
HEGP - clinical investigation centerParisFrance1
HEGP - physiology departmentParisFrance1