Acetate supplementation restores cognitive deficits caused by ARID1A haploinsufficiency in excitatory neurons
Abstract Mutations in AT‐rich interactive domain‐containing protein 1A (ARID1A) cause Coffin‐Siris syndrome (CSS), a rare genetic disorder that results in mild to severe intellectual disabilities. However, the biological role of ARID1A in the brain remains unclear. In this study, we report that the...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Springer Nature
2022-12-01
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Series: | EMBO Molecular Medicine |
Subjects: | |
Online Access: | https://doi.org/10.15252/emmm.202215795 |