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Journal of Neurology
Published in: Journal of Neurology 2/2013

01-02-2013 | Letter to the Editors

Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation

Authors: Una-Marie Sheerin, Maria Stamelou, Gavin Charlesworth, Tamara Shiner, Sian Spacey, Enza-Maria Valente, Nicholas W. Wood, Kailash P. Bhatia

Published in: Journal of Neurology | Issue 2/2013

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Excerpt

Dear Sirs, …
Literature
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Cao L, Huang XJ, Zheng L, Xiao Q, Wang XJ, Chen SD (2012) Identification of a novel PRRT2 mutation in patients with paroxysmal kinesigenic dyskinesias and c.649dupC as a mutation hot-spot. Parkinsonism Relat Disord 18(5):704–706
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Spacey SD, Valente EM, Wali GM, Warner TT, Jarman PR, Schapira AH, Dixon PH, Davis MB, Bhatia KP, Wood NW (2002) Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene. Mov Disord 17:717–725
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Metadata
Title
Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation
Authors
Una-Marie Sheerin
Maria Stamelou
Gavin Charlesworth
Tamara Shiner
Sian Spacey
Enza-Maria Valente
Nicholas W. Wood
Kailash P. Bhatia
Publication date
01-02-2013
Publisher
Springer-Verlag
Published in
Journal of Neurology / Issue 2/2013
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-012-6747-4

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