Article
Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations.
European journal of neurology - 1 Apr 2014
Tan L C S, Methawasin K, Teng E W L, Ng A R J, Seah S H, Au W L, Liu J J, Foo J N, Zhao Y, Tan E K
Abstract excerpt
BACKGROUND AND PURPOSE: Mutations in the PRRT2 gene have been identified in patients with paroxysmal kinesigenic dyskinesias (PKD); however, not many detailed clinico-genetic correlations have been performed. METHODS: To investigate PRRT2 mutations in a mixed Asian PKD population and perform clinico-genetic correlations, we recruited patients between 2002 and 2011 and administered a standardized questionnaire....
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