GABRB3 mutation as a cause of Ohtahara syndrome: A case report. Indian Journal of Case Reports, [S. l.], v. 7, n. 11, p. 480–481, 2021. DOI: 10.32677/ijcr.v7i11.3112. Disponível em: https://mansapublishers.com/ijcr/article/view/3112. Acesso em: 5 dec. 2025.