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Severe 5,10-methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia
A. Perna, M. Masciullo, A. Modoni, E. Cellini, E. Parrini, E. Ricci, A. M. Donati, G. Silvestri
Research output: Contribution to journal › Article › peer-review