FS are relatively common in GABAA receptor‐associated epilepsies caused by variants in GABRA1 (Johannesen et al., 2016; Maillard et al., 2022; Zhang & Liu, 2022), GABRB3 (Johannesen et al., 2022) or GABRG2 (Audenaert et al., 2006; Hancili et al., 2014; Hung et al., 2017). The gene discussed is GABRB3; the disease is epilepsy.