“…Li, Weidenfeld, & Morrisey, 2004). Despite these strong links to language, FOXP2 coding variants have not been directly associated with autism spectrum disorder (ASD) or specific language impairment (SLI; Marui et al, 2005; Newbury et al, 2002; Scott-Van Zeeland, Abrahams, et al, 2010; Toma et al, 2013), even though these disorders are also characterized by language deficits. In contrast, within a sample of dyslexic children and their unaffected relatives, a single nucleotide polymorphism (T vs. C) in an intron of FOXP2 , identified as rs7782412, was correlated with nonword repetition (NWR) score (Peter et al, 2011), with the major allele (T, frequency of 0.558) being associated with impairment on this task.…”