Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

Neurobiology of speech and language has previously been studied in the KE family, in which half of the members have severe impairment in both speech and language. The gene responsible for the phenotype was mapped to chromosome 7q31 and identified as the FOXP2 gene, coding for a transcription factor...

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Bibliografiske detaljer
Main Authors:	Shu, Weiguo, Cho, Julie Y., Jiang, Yuhui, Zhang, Minhua, Weisz, Donald, Elder, Gregory A., Schmeidler, James, De Gasperi, Rita, Sosa, Miguel A. Gama, Rabidou, Donald, Santucci, Anthony C., Perl, Daniel, Morrisey, Edward, Buxbaum, Joseph D.
Format:	Artigo
Sprog:	Inglês
Udgivet:	National Academy of Sciences 2005
Fag:	Biological Sciences
Online adgang:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1160518/ https://ncbi.nlm.nih.gov/pubmed/15983371 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0503739102
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Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

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