No association between SCN9A and monogenic human epilepsy disorders. (2020)

First Author: Fasham J
Attributed to:  Precision Medicine Exeter Innovation Platform (PMEI Platform) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1371/journal.pgen.1009161

PubMed Identifier: 33216760

Publication URI: http://europepmc.org/abstract/MED/33216760

Type: Journal Article/Review

Volume: 16

Parent Publication: PLoS genetics

Issue: 11

ISSN: 1553-7390