Li D et al.GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.Am J Hum Genet. 2016;99(4):802-816. PMID: 27616483.
XiangWei W et al.Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.Brain. 2019;142(10):3009-3027. PMID: 31504254.
