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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
WiTNNess - TNNT1 Myopathy Natural History Studycongenital structural myopathy, hereditary skeletal muscle disorder, muscle tissue disorder, musculoskeletal system disorder, nemaline myopathy, nemaline myopathy 5, nervous system disorder, neuromuscular diseaseRecruitingNot stated2026-06-23NCT06374719