Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

Title	Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum
Publication Type	Journal Article
Year of Publication	2007
Authors	Stevanin, G, Santorelli, FM, Azzedine, H, Coutinho, P, Chomilier, J, Denora, PS, Martin, E, Ouvrard-Hernandez, A-M, Tessa, A, Bouslam, N, Lossos, A, Charles, P, Loureiro, JL, Elleuch, N, Confavreux, C, Cruz, VT, Ruberg, M, Leguern, E, Grid, D, Tazir, M, Fontaine, B, Filla, A, Bertini, E, Durr, A, Brice, A
Journal	Nature Genetics
Volume	39
Issue	3
Pagination	366 - 372
Date Published	2007///
URL	http://www.scopus.com/inward/record.url?eid=2-s2.0-33847298447&partnerID=40&md5=0779140ab249f37e1319ab4044d3897d

Search form