The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function. (2021)

First Author: Jones LB

Attributed to: MRC Centre for Neurodevelopmental Disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3389/fphar.2021.788192

PubMed Identifier: 34925043

Publication URI: http://europepmc.org/abstract/MED/34925043

Type: Journal Article/Review

Volume: 12

Parent Publication: Frontiers in pharmacology

ISSN: 1663-9812