About: Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum   Goto Sponge  NotDistinct  Permalink

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  • Stevanin Giovanni, Azzedine Hamid, Coutinho Paula, Chomilier Jacques, Denora Paola, Ouvrard-Hernandez Anne-Marie, Tessa Alessandra, Bouslam Naima, Lossos Alexander, Charles Perrine, Loureiro José, Elleuch Nizar, Confavreux Christian, Ruberg Merle, Leguern Eric, Grid Djamel, Tazir Meriem, Fontaine Bertrand, Filla Alessandro, Bertini Enrico, Durr Alexandra, Brice Alexis. Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nature Genetics, Nature Publishing Group, 2007, 39 (3), pp.366 - 372. ⟨10.1038/ng1980⟩
Title
  • Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum
dc:date
  • 2007
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