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Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia
Author(s) -
Bhatia Kailash P.,
Schneider Susanne A.
Publication year - 2012
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.25038
Subject(s) - paroxysmal dyskinesia , genetics , exome sequencing , gene , channelopathy , candidate gene , epilepsy , exome , choreoathetosis , medicine , biology , dyskinesia , disease , mutation , neuroscience , dystonia , parkinson's disease
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