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Singing Mice, Songbirds, and More: Models for FOXP2 Function and Dysfunction in Human Speech and Language
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis of an inherited speech and language disorder suffered by members of the family known as “KE.” This mini-symposium review focuses on recent findings and research-in-progress, primarily from five labor...
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| Главные авторы: | , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Society for Neuroscience
2006
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2683917/ https://ncbi.nlm.nih.gov/pubmed/17035521 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3379-06.2006 |
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