Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleNovel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism.AuthorsGuidubaldi, Arianna; Piano, Carla; Santorelli, Filippo M.; Silvestri, Gabriella; Petracca, Martina; Tessa, Alessandra; Bentivoglio, Anna RitaPublicationMovement Disorders, 2011, Vol 26, Issue 3, p553ISSN0885-3185Publication typeArticleDOI10.1002/mds.23552