PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. (2012)
Attributed to:
ERANET 1 NEURON 3: Identification of copy number variants in familial and pathologically proven PD
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0b013e3182752c5a
PubMed Identifier: 23077024
Publication URI: http://europepmc.org/abstract/MED/23077024
Type: Journal Article/Review
Volume: 79
Parent Publication: Neurology
Issue: 21
ISSN: 0028-3878