Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum
Nature Genetics2007Vol. 39(3), pp. 366–372
Citations Over TimeTop 10% of 2007 papers
Giovanni Stévanin, Filippo M. Santorelli, Hamid Azzedine, Paula Coutinho, Jacques Chomilier, Paola S. Denora, Elodie Martin, Anne Marie Ouvrard-Hernandez, Alessandra Tessa, Naïma Bouslam, Alexander Lossos, Perrine Charles, José Leal Loureiro, Nizar Elleuch, Christian Confavreux, Vítor Tedim Cruz, Merle Ruberg, Éric Leguern, Djamel Grid, Mériem Tazir, Bertrand Fontaine, Alessandro Filla, Enrico Bertini, Alexandra Dürr, Alexis Brice
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