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

First Author: Fasham J

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

Parent Publication: PLOS Genetics

Issue: 11

ISSN: 1553-7390