Progressive myoclonus epilepsy KCNC1 variant causes a developmental dendritopathy. (2021)
Attributed to:
EnCRISPrx - A Permanent CRISPR-based Approach To Rescue Dravet Syndrome By Enhancing Scn1a Promoter Activity
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/epi.16867
PubMed Identifier: 33735526
Publication URI: http://europepmc.org/abstract/MED/33735526
Type: Journal Article/Review
Volume: 62
Parent Publication: Epilepsia
Issue: 5
ISSN: 0013-9580