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Nature Communications|July 15, 2022
SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in miceSalima El Chehadeh, Kyung Ah Han, Dongwook Kim, et al.American Journal of Human Genetics|January 22, 2026
MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathyHeba Morsy, Hyeonho Kim, Gyubin Jang, et al.Pageof 2