A significant step in this direction are recent studies that adapted the EEG technique in mice and show remarkably similar EEG phenotypes in Fmr1 KO mouse and humans with FXS [64], and a compelling alignment of sensory phenotypes in both humans with FXS and Fmr1 KO mice using an analogous visual discrimination tasks [117, 158]. The gene discussed is FMR1; the disease is fragile X syndrome.