Altered social behavior in mice carrying a cortical Foxp2 deletion

Genetic disruptions of the forkhead box transcription factor FOXP2 in humans cause an autosomal-dominant speech and language disorder. While FOXP2 expression pattern are highly conserved, its role in specific brain areas for mammalian social behaviors remains largely unknown. Here we studied mice ca...

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Publicado en:Hum Mol Genet
Main Authors: Medvedeva, Vera P, Rieger, Michael A, Vieth, Beate, Mombereau, Cédric, Ziegenhain, Christoph, Ghosh, Tanay, Cressant, Arnaud, Enard, Wolfgang, Granon, Sylvie, Dougherty, Joseph D, Groszer, Matthias
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2019
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General Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6381386/
https://ncbi.nlm.nih.gov/pubmed/30357341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy372
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