FOXP1 and language disorder: Taken together, five FOXP1 single gene deletions (Carr et al. 2010; Hamdan et al. 2010; Horn et al. 2010), two intragenic nonsense and frameshift mutations (Hamdan et al. 2010; O’Roak et al. 2011) and a chromosomal breakpoint disrupting FOXP1 supported by secondary CNV analysis (Talkowski et al. 2012) in patients with intellectual disability, ASD, language disorder and motor development delay, provide strong evidence for FOXP1 underlying various cognitive phenotypes (summarised in Table 2).