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...
Hoofdauteurs: | , , , , , , , , , |
---|---|
Formaat: | Artikel |
Taal: | English |
Gepubliceerd in: |
Springer Nature
2022-11-01
|
Reeks: | EMBO Molecular Medicine |
Onderwerpen: | |
Online toegang: | https://doi.org/10.15252/emmm.202215795 |