A structurally precise mechanism links an epilepsy-associated
Publication/Presentation Date
1-16-2024
Abstract
De novo heterozygous variants in
Volume
121
Issue
3
First Page
2307776121
Last Page
2307776121
ISSN
1091-6490
Published In/Presented At
Clatot, J., Currin, C. B., Liang, Q., Pipatpolkai, T., Massey, S. L., Helbig, I., Delemotte, L., Vogels, T. P., Covarrubias, M., & Goldberg, E. M. (2024). A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction. Proceedings of the National Academy of Sciences of the United States of America, 121(3), e2307776121. https://doi.org/10.1073/pnas.2307776121
Disciplines
Medicine and Health Sciences | Pediatrics
PubMedID
38194456
Department(s)
Department of Pediatrics
Document Type
Article
COinS