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

First Author: Papandreou A
Attributed to:  A gene therapy approach to childhood parkinsonism funded by MRC

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