Associated Papers
Two de novo GluN2B mutations affect multiple NMDAR-functions and instigate severe pediatric encephalopathy.
Kellner S et al.
Elife, 2021
34212862 (PubMed )
Supplement: elife-67555-supp2.xlsx › ClinVar_-_filtered
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Rodin RE et al.
Nature Neuroscience, 2021
33432195 (PubMed )
Supplement: NIHMS1648954-supplement-1648954_SuppTables.xlsx › Table_S7.2
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