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Generation of mice with a conditional Foxp2 null allele

Disruptions of the human FOXP2 gene cause problems with articulation of complex speech sounds, accompanied by impairment in many aspects of language ability. The FOXP2/Foxp2 transcription factor is highly similar in humans and mice, and shows a complex conserved expression pattern, with high levels...

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Detalhes bibliográficos
Main Authors: French, Catherine A, Groszer, Matthias, Preece, Christopher, Coupe, Anne-Marie, Rajewsky, Klaus, Fisher, Simon E
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley Subscription Services, Inc., A Wiley Company 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2682329/
https://ncbi.nlm.nih.gov/pubmed/17619227
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvg.20305
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