Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation. (2013)
Attributed to:
A systematic investigation into the pathogenesis and course of Parkinson's syndrome
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s00415-012-6747-4
PubMed Identifier: 23180180
Publication URI: http://europepmc.org/abstract/MED/23180180
Type: Journal Article/Review
Volume: 260
Parent Publication: Journal of neurology
Issue: 2
ISSN: 0340-5354