Identification of a novel variant p.Ser606Gly in SCN3A associated with childhood absence epilepsy. Li W, Zhao W, Wang J, Zhang X, et al. Epilepsy Res 2021;175:106682.

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Amedeo Smart

Independent Medical Education

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Li W, Zhao W, Wang J, Zhang X, et al. Identification of a novel variant p.Ser606Gly in SCN3A associated with childhood absence epilepsy. Epilepsy Res 2021;175:106682.
PMID: 34102392