ATP1A3 related disease manifesting as rapid onset dystonia-parkinsonism with prominent myoclonus and exaggerated startle
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference6 articles.
1. Heterogeneity of presentation and outcome in the Irish rapid-onset dystonia-Parkinsonism kindred;McKeon;Mov. Disord.,2007
2. Rapid-onset dystonia-parkinsonism;Dobyns;Neurology,1993
3. A neurophysiological study of myoclonus in patients with DYT11 myoclonus-dystonia syndrome;Marelli;Mov. Disord.,2008
4. Immunofluorescent localization of three Na,K-ATPase isozymes in the rat central nervous system: both neurons and glia can express more than one Na,K-ATPase;McGrail;J. Neurosci.,1991
5. Region- and neuronal-subtype-specific expression of Na,K-ATPase alpha and beta subunit isoforms in the mouse brain;Murata;J. Comp. Neurol.,2020
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