Mutations of N-Methyl-D-Aspartate Receptor Subunits in Epilepsy
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Physiology,General Neuroscience
Link
http://link.springer.com/article/10.1007/s12264-017-0191-5/fulltext.html
Reference75 articles.
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3. Yuan H, Low CM, Moody OA, Jenkins A, Traynelis SF. Ionotropic GABA and glutamate receptor mutations and human neurologic diseases. Mol Pharmacol 2015, 88: 203–217.
4. Wei F, Yan LM, Su T, He N, Lin ZJ, Wang J, et al. Ion channel genes and epilepsy: functional alteration, pathogenic potential, and mechanism of epilepsy. Neurosci Bull 2017, 33: 455–477.
5. Burnashev N, Szepetowski P. NMDA receptor subunit mutations in neurodevelopmental disorders. Curr Opin Pharmacol 2015, 20: 73–82.
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