Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries https://www.medrxiv.org/content/10.1101/2023.02.22.23286310
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries https://www.medrxiv.org/content/10.1101/2023.02.22.23286310