Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia

Emily C. Oates, Alexander M. Rossor, Majid Hafezparast, Michael Gonzalez, Fiorella Speziani, Daniel G. Macarthur, Monkol Lek, Ellen Cottenie, Mariacristina Scoto, A. Reghan Foley, Matthew Hurles, Henry Houlden, Linda Greensmith, Michaela Auer-Grumbach, Thomas R. Pieber, Tim M. Strom, Rebecca Schule, David N. Herrmann, Janet E. Sowden, Gyula AcsadiManoj P. Menezes, Nigel F. Clarke, Stephan Züchner, Francesco Muntoni, Kathryn N. North, Mary M. Reilly

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