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Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation. (2013)

First Author: Sheerin UM

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