Electrophysiological features of SYT2 mutations; a novel and treatable neuromuscular syndrome

by Whittaker, Roger G., Herrmann, David N., Bansagi, Boglarka, Hasan, Bashar Awwad Shiekh, Lofra, Robert Muni, Logigian, Eric L., Sowden, Janet E., Almodovar, Jorge L., Zuchner, Stephan, Horvath, Rita, Lochmüller, Hanns, Littleton, J. Troy
Published 2017

Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy

by Herrmann, David N, Horvath, Rita, Sowden, Janet E, Gonzales, Michael, Sanchez-Mejias, Avencia, Whittaker, Roger G, Almodovar, Jorge L, Lane, Maria, Bansagi, Boglarka, Pyle, Angela, Boczonadi, Veronika, Lochmüller, Hanns, Griffin, Helen, Chinnery, Patrick F, Lloyd, Thomas E, Zuchner, Stephan, Guan, Zhuo, Littleton, J. Troy
Published 2017