Familial cortical myoclonus with a mutation in NOL3.
Russell, Jonathan F.; Steckley, Jamie L.; Coppola, Giovanni; G. Hahn, Angelika F.; Howard, MacKenzie A.; Kornberg, Zachary; Huang, Alden; Mirsattari, Seyed M.; Merriman, Barry; Klein, Eric; Choi, Murim; Lee, Hsien-Yang; Kirk, Andrew; Nelson-Williams, Carol; Gibson, Gillian; Baraban, Scott C.; Lifton, Richard P.; Geschwind, Daniel H.; Fu, Ying-Hui; Ptáček, Louis J.; Annals of Neurology, 2012, vol. 72, issue 2, p 175, ISSN 03645134. ISBN 15318249.

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