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The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13.
Rapid onset dystonia-parkinsonism in a 14-year-old girl.
Rapid-onset dystonia-parkinsonism in a second family.
Variable phenotype of rapid-onset dystonia-parkinsonism.
Autosomal dominant torsion dystonia with onset in infancy.
Refined linkage to the RDP/DYT12 locus on 19q13.2 and evaluation of GRIK5 as a candidate gene.
Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonism.
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
Rapid-onset dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two families.
Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome?