FOXP2 is a gene that encodes a protein belonging to the forkhead box (FOX) family of transcription factors. It is primarily associated with language and speech development in humans. The gene is located on chromosome 7 and has been studied extensively in the context of human communication abilities. Mutations in the FOXP2 gene have been linked to language and speech disorders, particularly a condition known as specific language impairment (SLI).

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