DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Hoffman-Zacharska D, Szczepanik E, Terczynska I. et al.
From focal epilepsy to Dravet syndrome: heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit.
Neurol Neurochir Pol 2015;
49 (04) 258-266
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