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Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update.
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Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.
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Opposing Effects on Na1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures.
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SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.
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