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  1. A Study among the Genotype, Functional Alternations, and Phenotype of 9 SCN1A Mutations in Epilepsy Patients  / Kluckova D., Kolnikova M., Lacinova L. et al. .  Scientific reports . - volume 10, Article number: 10288 (2020)   [Dokument nie je vo fonde knižnice]
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