📣 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.

Delineation of the movement disorders associated with FOXG1 mutations. (2016)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000002585

PubMed Identifier: 27029630

Publication URI: http://europepmc.org/abstract/MED/27029630

Type: Journal Article/Review

Volume: 86

Parent Publication: Neurology

Issue: 19

ISSN: 0028-3878