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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
The Experience of Screening for SCIDCongenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA repair disease, Infant, Newborn, Diseases, Nutritional and Metabolic Diseases, Primary Immunodeficiency Diseases, hereditary disease, immune system disorder, inborn error of immunity, metabolic disease, severe combined immunodeficiencyRecruitingNot stated2022-12-14NCT05651113

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Research sitesCityCountryLinked trials
King's College LondonLondonUnited Kingdom1