Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration
scientific article published on 13 December 2007
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author: Giovanni Stevanin, José L. Loureiro, Mathieu Anheim, Paula Coutinho, Chokri Mhiri, Paulo Alegria, Christine Tranchant, Alexandra Durr, Alexis Brice, Didier Hannequin, Filippo Maria Santorelli, Christel Depienne, Amir Boukhris, Imed Feki, Sylvie Forlani, Vítor T. Cruz, Cyril Goizet, Chantal M E Tallaksen, Isabelle Le Ber, Hamid Azzedine, Anne Kjersti Erichsen, Meriem Tazir, Alexander Lossos, Abdelmadjid Hamri, Israela Lerer, Paola S Denora, Jérémy Truchetto, Florence Pasquier, Masatoyo Nishizawa, Soraya Belarbi
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