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Article

Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.

Neurology - 4 Aug 2009

Anselm I A, Sweadner K J, Gollamudi S, Ozelius L J, Darras B T

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Identifiers

PMID: 19652145
DOI: 10.1212/WNL.0b013e3181b04acd
PMCID: PMC2833268

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Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.PMID 19652145Read ↗

A novel de-novo mutation in the ATP1A3 gene causing 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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ATP1A3 mutation in rapid-onset dystonia parkinsonism: New data and genotype-phenotype correlation analysisSemantic proximity Read ↗

Atypical presentation of rapid-onset dystonia-parkinsonism in a toddler with a novel mutation in the ATP1A3 gene.Semantic proximity Read ↗

ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.Semantic proximity Read ↗

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

The diagnostic spectrum of ATP1A3-related disorders: 3 new patients.Semantic proximity Read ↗

[A childhood-onset rapid-onset dystonia parkinsonism family with ATP1A3 gene mutation and literatures review].Semantic proximity Read ↗

A novel presentation of an ATP1A3 gene mutation - case report and literature review.Semantic proximity Read ↗

ATP1A3-related disorders: An update.Semantic proximity Read ↗

Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations.Semantic proximity Read ↗

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