Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. (2022)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/epi.17166
PubMed Identifier: 35032048
Publication URI: http://europepmc.org/abstract/MED/35032048
Type: Journal Article/Review
Volume: 63
Parent Publication: Epilepsia
Issue: 3
ISSN: 0013-9580