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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2Charcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathyRecruitingNot stated2025-10-07NCT01193088