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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genetic Diagnosis in Inborn Errors of MetabolismLeber hereditary optic neuropathy, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, epilepsy, inborn mitochondrial metabolism disorder, metabolic disease, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular diseaseEnrolling by invitationNot stated2026-05-28NCT06376279

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Karolinska Institutet493
Region Stockholm164

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