Shopova, A. (2019) “Familial persistent hyperinsulinemic hypoglycemia with ABCC8 (SUR1) gen mutation with symptomatic epilepsy and mental retardation”, Bulgarian Neurology. Sofia, Bulgaria, 20(1), pp. 31–34. Available at: https://www.nevrologiabg.com/journal/index.php/neurology/article/view/77 (Accessed: 24 October 2026).