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Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).
Genetic links between brain development and brain evolution.
Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations.
Transmitral flow velocity in symptomatic severe aortic regurgitation: utility of Doppler for determination of preclosure of the mitral valve.
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
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Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. Neuron. 2004 Jul 22; 43(2):169-75.
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PubMed
subject areas
Amino Acid Sequence
Cell Line
Dystonia
Humans
Molecular Conformation
Mutation, Missense
Parkinsonian Disorders
Sodium-Potassium-Exchanging ATPase
Structure-Activity Relationship
authors with profiles
William B. Dobyns