IQSEC2 mutation update and review of the female-specific phenotype spectrum including intellectual disability and epilepsy. (2019)
Attributed to:
The role of NMDA receptor dysfunction in epileptic disorders
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.23670
PubMed Identifier: 30328660
Publication URI: http://europepmc.org/abstract/MED/30328660
Type: Journal Article/Review
Volume: 40
Parent Publication: Human mutation
Issue: 1
ISSN: 1059-7794