N., R.; J., P.; A., S. Heterozygous SLC1A2 mutation in a child with early infantile seizures and global developmental delay. International Journal of Contemporary Pediatrics, [S. l.], v. 9, n. 3, p. 299–302, 2022. DOI: 10.18203/2349-3291.ijcp20220460. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/4748. Acesso em: 28 feb. 2026.