Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice
Background: Epigenetic disruptions have been implicated in neurodevelopmental disorders. NSD2 is associated with developmental delay/intellectual disability; however, its role in brain development and function remains unclear.Methods: We performed transcriptomic and epigenetic analyses using Nsd2 kn...
| Published in: | Frontiers in Genetics |
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| Main Authors: | , , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2024-02-01
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| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2024.1308234/full |
