Autosomal dominant hereditary spastic paraplegia: report of a large italian family with R581X spastin mutation.
- Authors: ARIDON P; RAGONESE P; DE FUSCO M; LO COCO D; SALEMI G; CASARI G; SAVETTIERI G
- Publication year: 2007
- Type: Articolo in rivista
- OA Link: http://hdl.handle.net/10447/13380