📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. (2012)

First Author: Gardiner AR

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