YILMAZ, H. Önder. Homozygous SCN2A gene mutation causing early infantile epileptic encephalopathy: The second case in literature. Medical Science and Discovery, [S. l.], v. 6, n. 9, p. 221–223, 2019. DOI: 10.36472/msd.v6i9.302. Disponível em: https://www.medscidiscovery.com/index.php/msd/article/view/302. Acesso em: 3 oct. 2022.