Asystole in alternating hemiplegia with de novo ATP1A3 mutation
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
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4. Mutations in the Na+/K+-ATPase α3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism;de Carvalho Aguiar;Neuron,2004
5. Alternating hemiplegia of childhood;Gordon;Dev Med Child Neurol,1995
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