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Phenotypic overlap among paroxysmal dyskinesia subtypes: Lesson from a family with PRRT2 gene mutation

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第一作者： Wang,K.

作者： Wang,K. ^[1] ; Zhao,X. ^[2] ; Du,Y. ; He,F. ; Peng,G. ; Luo,B.

作者单位： Brain Medical Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, China ^[1] Department of Neurology, The First Affiliated Hospital, School of Medicine, Zhejiang University ^[2]

关键词 Familial occurrence Paroxysmal dyskinesia Phenotype PRRT2 Trigger

发布时间 2013-11-20

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Brain & Development

2013年35卷7期

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Brain & Development

2013年35卷7期

664-666页

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Phenotypic overlap among paroxysmal dyskinesia subtypes: Lesson from a family with PRRT2 gene mutation

Brain & Development

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Phenotypic overlap among paroxysmal dyskinesia subtypes: Lesson from a family with PRRT2 gene mutation

Brain & Development

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Brain & Development

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