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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Detalhes bibliográficos
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.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2005
Assuntos:
Biological Sciences
Acesso em linha: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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