Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations-Reference-Cited by-同舟云学术

Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations

Published:2013-03-29 Issue:4 Volume:21 Page:674-678
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Tan L. C. S.¹²,Methawasin K.¹²,Teng E. W. L.²,Ng A. R. J.²,Seah S. H.¹²,Au W. L.¹²,Liu J. J.³,Foo J. N.³,Zhao Y.⁴,Tan E. K.¹²

Affiliation:

1. Parkinson's Disease and Movement Disorders Centre; USA National Parkinson Foundation Centre of Excellence, National Neuroscience Institute; Singapore City Singapore

2. Department of Neurology; National Neuroscience Institute; Singapore City Singapore

3. Human Genetics; Genome Institute of Singapore; A*STAR; Singapore City Singapore

4. Department of Clinical Research; Singapore General Hospital; Singapore City Singapore

Funder

Singapore Millennium Foundation

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ene.12142/fullpdf

Reference20 articles.

1. Paroxysmal dyskinesias;Bhatia;Mov Disord,2011

2. Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia;Chen;Nat Genet,2011

3. Mutations in the novel protein PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions;Lee;Cell Rep,2012

4. PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome;Heron;Am J Hum Genet,2012

5. PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine;Gardiner;Neurology,2012

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