Associated Papers
Scanning mutagenesis of the voltage-gated sodium channel NaV1.2 using base editing.
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Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders.
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Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
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Lacosamide for SCN2A-related intractable neonatal and infantile seizures.
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Epileptic Disorders : International Epilepsy Journal With Videotape, 2018
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