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Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain
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“Individuals with FOXP2 mutations have dominantly inherited verbal dyspraxia and linguistic and/ or grammatical difficulties.(2,4,5) Additionally, patients with FOXP2 mutations have demonstrated developmental abnormalities of the basal ganglia (BG) and inferior frontal cortex (IFC).”
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Metadata
- Authors
- Spiteri, E., Konopka, G., Coppola, G., Bomar, J., Oldham, M., Ou, J., Vernes, S. C., Fisher, S. E., Ren, B., & Geschwind, D. H.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2007-12
- Volume
- 81
- Issue
- 6
- Pages
- 1144-1157
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2109245019
- Cited by
- 285
- References
- 90
- FWCI
- 9.04
- Type
- journal article
- Language
- en
- Open access
- bronze
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