Associated Papers
Synaptic dysregulation in a mouse model of GRIN2D developmental and epileptic encephalopathy.
Teoh J et al.
Brain : a Journal of Neurology, 2025
Clinical whole genome sequencing in pediatric epilepsy: Genetic and phenotypic spectrum of 733 individuals.
Henry OJ et al.
Epilepsia, 2025
40183601 (PubMed )
Supplement: EPI-66-2966-s001.xlsx › supplementary_table9_v2.01
Genetic aetiologies in relation to response to the ketogenic diet in 226 children with epilepsy.
Dahlin M et al.
Brain Communications, 2025
40290421 (PubMed )
Supplement: fcaf134_supplementary_data.zip › Dahlin_et_al._Supplementary_table_3_revised.xlsx › Bara_EP
Identification of a novel GRIN2D variant in a neonate with intractable epileptic encephalopathy-a case report.
Jiao J et al.
Bmc Pediatrics, 2021
Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.
XiangWei W et al.
Brain : a Journal of Neurology, 2019
GRIN2D variants in three cases of developmental and epileptic encephalopathy.
Tsuchida N et al.
Clinical Genetics, 2018
Select a paper to view details