Mutations and modeling of the chromatin remodeler CHD8 define an emerging autism etiology
Autism Spectrum Disorder (ASD) is a common neurodevelopmental disorder with a strong but complex genetic component. Recent family based exome-sequencing strategies have identified recurrent de novo mutations at specific genes, providing strong evidence for ASD risk, but also highlighting the extreme...
| Հիմնական հեղինակներ: | , , |
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| Ձևաչափ: | Հոդված |
| Լեզու: | English |
| Հրապարակվել է: |
Frontiers Media S.A.
2015-12-01
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| Շարք: | Frontiers in Neuroscience |
| Խորագրեր: | |
| Առցանց հասանելիություն: | http://journal.frontiersin.org/Journal/10.3389/fnins.2015.00477/full |