Associated Papers
GRIN2B-related neurodevelopmental disorders: genotype-phenotype correlations and therapeutic implications.
Xie C et al.
Orphanet Journal of Rare Diseases, 2025
41146259 (PubMed )
Supplement: 13023_2025_4055_MOESM1_ESM.xlsx › Supplementary_table1
L-serine treatment in patients with GRIN-related encephalopathy: a phase 2A, non-randomized study.
Juliá-Palacios N et al.
Brain : a Journal of Neurology, 2024
Identification of homologous GluN subunits variants accelerates GRIN variants stratification.
Santos-Gómez A et al.
Frontiers in Cellular Neuroscience, 2022
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