Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. (2013)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/dmcn.12056
PubMed Identifier: 23363396
Publication URI: http://europepmc.org/abstract/MED/23363396
Type: Journal Article/Review
Volume: 55
Parent Publication: Developmental medicine and child neurology
Issue: 4
ISSN: 0012-1622