The finding of the same language deficit in half the members of the KE family is taken as suggesting that a specific allele (FOXP2) is normally involved in the development of language. Recent studies, however, question the exclusivity of FOXP2, and it is argued that the finding of a gene that disrupts language should not be taken as strong evidence for the existence of genes that underlie it.
Email your librarian or administrator to recommend adding this journal to your organisation's collection.
* Views captured on Cambridge Core between September 2016 - 29th June 2017. This data will be updated every 24 hours.