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/10.1038/s41593-024-01747-8
PubMed Identifier: 39363051
Publication URI: http://europepmc.org/abstract/MED/39363051
Type: Journal Article/Review
Volume: 27
Parent Publication: Nature neuroscience
Issue: 10
ISSN: 1097-6256