Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleFurther evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia.AuthorsMuglia, Maria; Magariello, Angela; Nicoletti, Giuseppe; Patitucci, Alessandra; Gabriele, Anna Lia; Conforti, Francesca Luisa; Mazzei, Rosalucia; Caracciolo, Manuela; Ardito, Bonaventura; Lastilla, Marcello; Tedeschi, Gioacchino; Quattrone, AldoPublicationAnnals of Neurology, 2002, Vol 51, Issue 6, p794ISSN0364-5134Publication typeArticleDOI10.1002/ana.10185