GRIN2D

Publications

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.