Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

Giovanni Stevanin, Hamid Azzedine, Paola Denora, Amir Boukhris, Meriem Tazir, Alexander Lossos, Alberto Luis Rosa, Israela Lerer, Abdelmadjid Hamri, Paulo Alegria, José Loureiro, Masayoshi Tada, Didier Hannequin, Mathieu Anheim, Cyril Goizet, Victoria Gonzalez-Martinez, Isabelle Le Ber, Sylvie Forlani, Kiyoshi Iwabuchi, Vardiela MeinerGoekhan Uyanik, Anne Kjersti Erichsen, Imed Feki, Florence Pasquier, Soreya Belarbi, Vitor T. Cruz, Christel Depienne, Jeremy Truchetto, Guillaume Garrigues, Chantal Tallaksen, Christine Tranchant, Masatoyo Nishizawa, José Vale, Paula Coutinho, Filippo M. Santorelli, Chokri Mhiri, Alexis Brice, Alexandra Durr

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