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High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language Disorders

We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication disorder, primarily characterized by difficulties in learning to make coordinated sequences of articulatory gestures that underlie speech. Affected people have deficits in expressive and receptive linguis...

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Detalhes bibliográficos
Main Authors: Vernes, Sonja C. , Spiteri, Elizabeth , Nicod, Jérôme , Groszer, Matthias , Taylor, Jennifer M. , Davies, Kay E. , Geschwind, Daniel H. , Fisher, Simon E. 
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Human Genetics 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2276341/
https://ncbi.nlm.nih.gov/pubmed/17999362
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