FOXP2 is a gene associated with autism and language disorders.
FOXP2 is a gene associated with autism and language disorders.
Lai and colleagues (2001) identified forkhead box P2 (FOXP2) as a causal gene for a severe speech and language disorder in a three-generation pedigree. Because language impairments are a hallmark of autism, the gene has been examined as a potential cause of the disorder. Results from two independent family studies, however, failed to find an association between FOXP2 and autism.