1. Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum. Issue 5 (5th February 2009) Authors: Crimella, C; Arnoldi, A; Crippa, F; Mostacciuolo, M L; Boaretto, F; Sironi, M; D'Angelo, M Grazia; Manzoni, S; Piccinini, L; Turconi, A C; Toscano, A; Musumeci, O; Benedetti, S; Fazio, R; Bresolin, N; Daga, A; Martinuzzi, A; Bassi, M T Journal: Journal of medical genetics Issue: Volume 46:Issue 5(2009) Page Start: 345 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗