FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
Disruption of FOXP2, a gene encoding a forkhead-domain transcription factor, causes a severe developmental disorder of verbal communication, involving profound articulation deficits, accompanied by linguistic and grammatical impairments. Investigation of the neural basis of this disorder has been li...
Päätekijät: | , , , , |
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Aineistotyyppi: | Journal article |
Kieli: | English |
Julkaistu: |
2003
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