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.
Hacıhamdioğlu B, Özgürhan G, Çaran B, Meydan-Aksanlı E, Keskin E.
Hacıhamdioğlu B, et al. Among authors: keskin e.
Turk J Pediatr. 2018;60(5):581-583. doi: 10.24953/turkjped.2018.05.018.
Turk J Pediatr. 2018.
PMID: 30968641
Free article.
Hacihamdioglu B, Ozgurhan G, Caran B, Meydan-Aksanli E, Keskin E. 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. ...
Hacihamdioglu B, Ozgurhan G, Caran B, Meydan-Aksanli E, Keskin E. Glycogen storage disease type 0 due to a novel frames …