Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: Report of three new mutations
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference12 articles.
1. Hepatic glycogen synthetase deficiency: definition of syndrome from metabolic and enzyme studies on a 9 year old girl;Aynsley-Green;Arch Dis Child,1977
2. Infantile hypoglycemia due to inherited deficiency of glycogen synthetase in liver;Lewis;Arch Dis Child,1963
3. Hepatic glycogen synthetase deficiency: further studies on a family;Dykes;Arch Dis Child,1972
4. Liver glycogen synthetase deficiency: a rarely diagnosed entity;Gitzelmann;Eur J Pediatr,1996
5. Liver glycogen synthase deficiency: a cause of ketotic hypoglycemia;Rutledge;Pediatrics,2001
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