FOXP2 as a molecular window into speech and language.
Rare mutations of the FOXP2 transcription factor gene cause a monogenic syndrome characterized by impaired speech development and linguistic deficits. Recent genomic investigations indicate that its downstream neural targets make broader impacts on common language impairments, bridging clinically di...
| Main Authors: | , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2009
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