Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNIPA1 ( SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.AuthorsKlebe, Stephan; Lacour, Arnaud; Durr, Alexandra; Stojkovic, Tanya; Depienne, Christel; Forlani, Sylvie; Poea-Guyon, Sandrine; Vuillaume, Isabelle; Sablonniere, Bernard; Vermersch, Patrick; Brice, Alexis; Stevanin, GiovanniPublicationNeurogenetics, 2007, Vol 8, Issue 2, p155ISSN1364-6745Publication typeLetterDOI10.1007/s10048-006-0074-9