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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
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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
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