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Frontiers in Pediatrics|December 16, 2021
Mechanisms of Congenital Myasthenia Caused by Three Mutations in the <i>COLQ</i> GeneXiaona Luo, Chunmei Wang, Longlong Lin, et al.Genes & Development|July 30, 2015
CaV3.2 calcium channels control NMDA receptor-mediated transmission: a new mechanism for absence epilepsyGuangfu Wang, Genrieta Bochorishvili, Yucai Chen, et al.Pageof 8