The Expanding Spectrum of Neurological Phenotypes in Children With ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond-Reference-Cited by-同舟云学术

The Expanding Spectrum of Neurological Phenotypes in Children With ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond

Published:2015-01 Issue:1 Volume:52 Page:56-64
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Sweney Matthew T.^ORCID,Newcomb Tara M.^ORCID,Swoboda Kathryn J.

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference73 articles.

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3. Rapid-onset dystonia-parkinsonism;Dobyns;Neurology,1993

4. Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism;de Carvalho Aguiar;Neuron,2004

5. Variable phenotype of rapid-onset dystonia-parkinsonism;Brashear;Mov Disord,1996

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