We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleExon deletions of SPG4 are a frequent cause of hereditary spastic paraplegiaAuthorsDepienne, Christel; Fedirko, Estelle; Forlani, Sylvie; Cazeneuve, Cécile; Ribaï, Pascale; Feki, Imed; Tallaksen, Chantal; Nguyen, Karine; Stankoff, Bruno; Ruberg, Merle; Stevanin, Giovanni; Durr, Alexandra; Brice, AlexisPublicationJournal of Medical Genetics (JMG), 2007, Vol 44, Issue 4, p281ISSN0022-2593Publication typearticle