The Turkish Journal of Pediatrics 2018 , Vol 60 , Num 5
Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia
Bülent Hacıhamdioğlu 1 ,Gamze Özgürhan 2 ,Bahar Çaran 2 ,Evrim Meydan-Aksanlı 2 ,Ece Keskin 3
1 Departments of Pediatric Endocrinology, University of Health Sciences, Suleymaniye Women Maternity and Child Diseases Training and Research Hospital, İstanbul, Turkey
2 Departments of Pediatrics, University of Health Sciences, Suleymaniye Women Maternity and Child Diseases Training and Research Hospital, İstanbul, Turkey
3 Departments of Medical Genetics, University of Health Sciences, Suleymaniye Women Maternity and Child Diseases Training and Research Hospital, İstanbul, Turkey
DOI : 10.24953/turkjped.2018.05.018 Keywords :
Copyright © 2016 turkishjournalpediatrics.org