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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Udgivet i:Front Behav Neurosci
Main Authors: Chabout, Jonathan, Sarkar, Abhra, Patel, Sheel R., Radden, Taylor, Dunson, David B., Fisher, Simon E., Jarvis, Erich D.
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2016
Fag:
Neuroscience
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5071336/
https://ncbi.nlm.nih.gov/pubmed/27812326
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnbeh.2016.00197
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