Enrolling by invitation
Imaging and Gait Analysis in FSHD Patients
NCT07164937
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, FSHD - Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
- Locations
-
- UOC Neurologia Rome, Italy