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