1.
Shopova A. Familial persistent hyperinsulinemic hypoglycemia with ABCC8 (SUR1) gen mutation with symptomatic epilepsy and mental retardation. NEU [Internet]. 2019 Jun. 30 [cited 2026 Oct. 23];20(1):31-4. Available from: https://www.nevrologiabg.com/journal/index.php/neurology/article/view/77