A human electrophysiological biomarker of Fragile X Syndrome is shared in V1 of Fmr1 KO mice and caused by loss of FMRP in cortical excitatory neurons

By Sara S. Kornfeld-Sylla, Cigdem Gelegen, J. E. Norris, Francesca A. Chaloner, Maia Lee, Michael Khela, Maxwell J Heinrich, Peter S. B. Finnie, Lauren E. Ethridge, Craig A. Erickson and 4 more. 2025

Subfields: Cellular and Molecular Neuroscience, Genetics, Neurology