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Neurology|August 29, 2025
Small Vessel Disease Phenotype Associated With Monoallelic <i>NOTCH3</i> Loss-of-Function VariantsJosephine S van Asbeck, Gido Gravesteijn, Minne N Cerfontaine, et al.Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.Pageof 2