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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Phenotypes, Biomarkers and Pathophysiology in Hereditary Spastic Paraplegias and Related DisordersCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathyRecruitingNot stated2021-05-19NCT03981276