Foxp2 Mutations Impair Auditory-Motor Association Learning

Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described examples of monogenic speech and language disorders. Acquisition of proficient spoken language involves auditory-guided vocal learning, a specialized form of sensory-motor association learning. The impact of...

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Detalles Bibliográficos
Autores principales: Kurt, Simone, Fisher, Simon E., Ehret, Günter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296769/
https://www.ncbi.nlm.nih.gov/pubmed/22412993
http://dx.doi.org/10.1371/journal.pone.0033130

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296769/
https://www.ncbi.nlm.nih.gov/pubmed/22412993
http://dx.doi.org/10.1371/journal.pone.0033130

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