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Article

Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia Parkinsonism

1 Jul 2004

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15260953
DOI: 10.1016/j.neuron.2004.06.028

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Related research

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Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia ParkinsonismPMID 15260953Read ↗

Distinct neurological disorders with ATP1A3 mutations.Semantic proximity Read ↗

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ATP1A3 Mutation in Adult Rapid-Onset Ataxia.Semantic proximity Read ↗

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ATP1A3-Associated Paroxysmal Dystonia.Semantic proximity Read ↗

The expanding clinical and genetic spectrum of ATP1A3-related disorders.Semantic proximity Read ↗

The Expanding Phenotypic Spectrums Associated with ATP1A3 Mutation in a Family with Rapid-Onset Dystonia Parkinsonism.Semantic proximity Read ↗

Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.Semantic proximity Read ↗

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