GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel BlockersDong Li, Marni J. Falk, Hongjie Yuan et al.|The American Journal of Human Genetics|2016Cited by 183
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Clinical features and genotype–phenotype correlations in epilepsy patients with de novo <scp><i>DYNC1H1</i></scp> variantsClaudia Cuccurullo, Hormos Salimi Dafsari, Emanuele Cerulli Irelli et al.|Epilepsia|2024Cited by 7
GRIN2B Encephalopathy: Novel FindingsJohannes R. Lemke, Hirofumi Kusumoto, Mark Mintz et al.|Unknown|2017Cited by 0