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A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland

  • Published:2015-01 Issue: Volume:1595 Page:120-126
  • ISSN:0006-8993
  • Container-title:Brain Research
  • language:en
  • Short-container-title:Brain Research

Author:

Liang Shuli,Yu Xiaoman,Zhang Shaohui,Tai Junli

Funder

Chinese National Nature & Science Foundation

Beijing Technology & Science New-star Training Project

Publisher

Elsevier BV

Subject

Developmental Biology,Clinical Neurology,Molecular Biology,General Neuroscience

Reference25 articles.

1. Paroxysmal dyskinesias;Bhatia;Mov. Disord.,2011

2. Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia;Bruno;Neurology,2007

3. Genomic structure of human anion exchanger 3 and its potential role in hereditary neurological disease;Einum;Neurogenetics,1998

4. Paroxysmal dystonic choreoathetosis:tight linkage to chromosome 2q;Fink;Am. J. Hum. Genet.,1996

5. Paroxysmal non-kinesigenic dyskinesia caused by the mutation of MR-1 in a large Polish kindred;Friedman;Eur. Neuro,2009

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