SHOPOVA, Ana. Familial persistent hyperinsulinemic hypoglycemia with ABCC8 (SUR1) gen mutation with symptomatic epilepsy and mental retardation. Bulgarian Neurology, Sofia, Bulgaria, v. 20, n. 1, p. 31–34, 2019. Disponível em: https://www.nevrologiabg.com/journal/index.php/neurology/article/view/77. Acesso em: 24 oct. 2026.