Article

Mice carrying a humanized <i>Foxp2</i> knock-in allele show region-specific shifts of striatal Foxp2 expression levels

2019-01-09

Abstract excerpt

<h4>ABSTRACT</h4> Genetic and clinical studies of speech and language disorders are providing starting points to unravel underlying neurobiological mechanisms. The gene encoding the transcription factor FOXP2 has been the first example of a gene involved in the development and evolution of this human-specific trait. A number of autosomal-dominant FOXP2 mutations are associated with developmental speech and lang...

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Literature Corpus work: 9358777a-026b-5819-ab29-19c56ed53934
DOI: 10.1101/514893

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