Mapping of Human FOXP2 Enhancers Reveals Complex Regulation
Mutations of the FOXP2 gene cause a severe speech and language disorder, providing a molecular window into the neurobiology of language. Individuals with FOXP2 mutations have structural and functional alterations affecting brain circuits that overlap with sites of FOXP2 expression, including regions...
| Những tác giả chính: | , , , |
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| Định dạng: | Bài viết |
| Ngôn ngữ: | English |
| Được phát hành: |
Frontiers Media S.A.
2018-02-01
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| Loạt: | Frontiers in Molecular Neuroscience |
| Những chủ đề: | |
| Truy cập trực tuyến: | http://journal.frontiersin.org/article/10.3389/fnmol.2018.00047/full |