Table 2.
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 |