Table 2.

List of Case with FOXP2 Disruptions Discussed in This Review

Case Description	Reference to the Paper(s) Describing the Genetic Cause for the Disorder
The affected members of the KE family, who had a diverse phenotype caused by a point mutation in FOXP2.	Lai et al.22
CS, who had verbal dyspraxia resulting from a translocation disrupting the FOXP2 gene.	Lai et al.22
Three non-synonymous mutations in children with developmental verbal dyspraxia.	MacDermot et al.25
Oromotor and verbal dyspraxia and developmental delay in a child carrying a FOXP2 deletion.	Zeesman et al.26
A loss of paternal FOXP2 in children with developmental verbal dyspraxia.	Feuk et al.27
A loss of maternal FOXP2 resulting in verbal dyspraxia.	Rice et al.28