Van Kerkhoven, C., L. Mumba, J. Harvengt, and J.-P. Misson. “Severe Hypotonia and Developmental Delay Due to an EBF3 Pathogenic Variant: Clinical Implications of a Molecular Defect and Narrative Review”. Belgian Journal of Paediatrics, vol. 26, no. 1, Apr. 2024, pp. 34-38, http://belgjpaediatrics.com/index.php/bjp/article/view/198.