MYATHARI, R.; GUPTA, A.; BIJARNIA-MAHAY, S. Novel mutation in DMN1L gene in child with Landau Kleffner syndrome: a rare association. International Journal of Contemporary Pediatrics, [S. l.], v. 9, n. 9, p. 855–859, 2022. DOI: 10.18203/2349-3291.ijcp20222127. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/4956. Acesso em: 6 nov. 2025.