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Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis
  1. Correspondence to Professor Ying Liu, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences; School of Basic Medicine, Peking Union Medical College, 5 Dongdan 3 Tiao, Beijing 100005, China; liuyingpumc{at}yahoo.com Professor Yuping Wang, Department of Neurology, Xuanwu Hospital, Capital Medical University, 45 Changchun Street, Beijing 100053, China; mdwangyp{at}yahoo.com.cn
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Li J, Zhu X, Wang X, et al
Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis

Publication history

  • Received November 17, 2011
  • Revised November 22, 2011
  • Accepted November 23, 2011
  • First published November 30, 2011.
Online issue publication 
January 12, 2012

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