| Title: |
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes |
| Authors: |
Chen, Siwei; Abou-Khalil, Bassel W.; Afawi, Zaid; Ali, Quratulain Zulfiqar; Amadori, Elisabetta; Anderson, Alison; Anderson, Joe; Andrade, Danielle M.; Annesi, Grazia; Arslan, Mutluay; Berkovic, Samuel F.; Epi25 Collaborative |
| Contributors: |
Chen, Siwei; Abou-Khalil, Bassel W.; Afawi, Zaid; Ali, Quratulain Zulfiqar; Amadori, Elisabetta; Anderson, Alison; Anderson, Joe; Andrade, Danielle M.; Annesi, Grazia; Arslan, Mutluay; Berkovic, Samuel F.; Epi25 Collaborative |
| Publication Year: |
2024 |
| Collection: |
Georg-August-Universität Göttingen: GoeScholar |
| Description: |
U.S. Department of Health & Human Services | National Institutes of Health https://doi.org/10.13039/100000002 ; U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute https://doi.org/10.13039/100000051 |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| Relation: |
1747 |
| DOI: |
10.1038/s41593-024-01747-8 |
| Availability: |
https://resolver.sub.uni-goettingen.de/purl?gro-2/147974; https://doi.org/10.1038/s41593-024-01747-8 |
| Rights: |
info:eu-repo/semantics/openAccess ; https://www.springernature.com/gp/researchers/text-and-data-mining |
| Accession Number: |
edsbas.7B7821AD |
| Database: |
BASE |