Cardiac phenotype in ATP1A3-related syndromes
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DOI: 10.1212/wnl.0000000000010794
Abstract: Objective To define the risks and consequences of cardiac abnormalities in ATP1A3-related syndromes. Methods Patients meeting clinical diagnostic criteria for rapid-onset dystonia-parkinsonism (RDP), alternating hemiplegia of childhood (AHC), and cerebellar ataxia, areflexia, pes cavus, optic… read more here.
Keywords: atp1a3 related; cardiac phenotype; phenotype atp1a3; related syndromes ... See more keywords