Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression
Intellectual disability (ID), autism, and epilepsy share frequent yet variable comorbidities with one another. In order to better understand potential genetic divergence underlying this variable risk, we studied genes responsible for monogenic IDs, grouped according to their autism and epilepsy como...
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| Huvudupphovsmän: | , , , , |
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| Materialtyp: | Artigo |
| Språk: | engelska |
| Publicerad: |
2016
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| Länkar: | https://doi.org/10.1186/s13229-016-0082-z https://molecularautism.biomedcentral.com/track/pdf/10.1186/s13229-016-0082-z |
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