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...

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Bibliografische gegevens
Hoofdauteurs: Pei‐Pei Liu, Shang‐Kun Dai, Ting‐Wei Mi, Gang‐Bin Tang, Zhuo Wang, Hui Wang, Hong‐Zhen Du, Yi Tang, Zhao‐Qian Teng, Chang‐Mei Liu
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