References:

1.Epi25 Collaborative. Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Nat Neurosci 2024; 27 (10): 1864–1879.

2.GeneCards website. https://www.genecards.org/. Accessed August 2025.

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Published 26.11.2025
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