AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disordersVincenzo Salpietro, Alison M. Muir, Kristin G. Monaghan et al.|Nature Communications|2019Cited by 248
Defining the phenotypic spectrum of <i>SLC6A1</i> mutationsKatrine M. Johannesen, Guido Rubboli, Boris Keren et al.|Epilepsia|2018Cited by 151