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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Follow-up Study on Female Carriers With DMD Gene VariantsBecker muscular dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseEnrolling by invitationNot stated2025-06-06NCT05715957

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Research sitesCityCountryLinked trials
Copenhagen neuromuscular centerCopenhagenDenmark1