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New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism.
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.
Psychiatric disorders in rapid-onset dystonia-parkinsonism.
KCNQ1 Potassium Channel
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.
Cognitive impairment in rapid-onset dystonia-parkinsonism.
ATP1A3 Mutation in Adult Rapid-Onset Ataxia.
Revising rapid-onset dystonia-parkinsonism: Broadening indications for ATP1A3 testing.
Auditory-perceptual voice and speech evaluation in ATP1A3 positive patients.