A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice

Development of proficient spoken language skills is disrupted by mutations of the FOXP2 transcription factor. A heterozygous missense mutation in the KE family causes speech apraxia, involving difficulty producing words with complex learned sequences of syllables. Manipulations in songbirds have hel...

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Detalles Bibliográficos
Autores principales: Chabout, Jonathan, Sarkar, Abhra, Patel, Sheel R., Radden, Taylor, Dunson, David B., Fisher, Simon E., Jarvis, Erich D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071336/
https://www.ncbi.nlm.nih.gov/pubmed/27812326
http://dx.doi.org/10.3389/fnbeh.2016.00197

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071336/
https://www.ncbi.nlm.nih.gov/pubmed/27812326
http://dx.doi.org/10.3389/fnbeh.2016.00197

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