📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. (2013)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.2728

PubMed Identifier: 23933819

Publication URI: http://europepmc.org/abstract/MED/23933819

Type: Journal Article/Review

Volume: 45

Parent Publication: Nature genetics

Issue: 9

ISSN: 1061-4036