Van Kerkhoven, C., Mumba, L., Harvengt, J., & Misson, J.-P. (2024). Severe hypotonia and developmental delay due to an EBF3 pathogenic variant: Clinical implications of a molecular defect and narrative review. Belgian Journal of Paediatrics, 26(1), 34–38. Retrieved from http://belgjpaediatrics.com/index.php/bjp/article/view/198