VAN KERKHOVEN, C.; MUMBA, L.; HARVENGT, J.; MISSON, J.-P. Severe hypotonia and developmental delay due to an EBF3 pathogenic variant: Clinical implications of a molecular defect and narrative review. Belgian Journal of Paediatrics, [S. l.], v. 26, n. 1, p. 34–38, 2024. Disponível em: https://mail.belgjpaediatrics.com/index.php/bjp/article/view/198. Acesso em: 17 apr. 2026.