Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. (2024)
Attributed to:
An integrated systems-level framework for deciphering multidrug resistant epilepsy.
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/2023.02.22.23286310
PubMed Identifier: 36865150
Publication URI: http://europepmc.org/abstract/MED/36865150
Type: Journal Article/Review
Parent Publication: medRxiv : the preprint server for health sciences