Coherently, mutations in POU3F3 (Snijders Blok et al., 2019), SATB2 (Bengani et al., 2017; Fu et al., 2022; Leoyklang et al., 2007), BCL11B (Lessel et al., 2018), or TBR1 (De Rubeis et al., 2014; Deriziotis et al., 2014) are associated with NDDs, including intellectual disability (ID) and autism spectrum disorder (ASD). The gene discussed is BCL11B; the disease is autism spectrum disorder.