Associated Papers
Modeling epilepsy by loss-of-function of the CUG-binding protein Elav-like family member 2 in zebrafish with multi-omics analysis.
Wang X et al.
Chinese Medical Journal, 2026
Genetic variants disrupting activity-dependent CELF2 shuttling cause neuronal hyperexcitability, learning deficits, and seizures.
Hua M et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
De novo variants in CELF2 that disrupt the nuclear localization signal cause developmental and epileptic encephalopathy.
Itai T et al.
Human Mutation, 2021
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