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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genetic Basis of ImmunodeficiencyCongenital, 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 stated2026-09-28NCT00055172

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Research sitesCityCountryLinked trials
National Institutes of Health Clinical CenterBethesdaUnited States800