Metabolic and Genetic Liver Diseases: Glycogen Storage Diseases
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-30103-7_22
Reference8 articles.
1. Bao Y et al. Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene. J Clin Invest. 1996;97(4):941–8.
2. Roscher A et al. The natural history of glycogen storage disease types VI and IX: long-term outcome from the largest metabolic center in Canada. Mol Genet Metab. 2014;113(3):171–6.
3. Ullrich K, Smit GP. Clinical aspects of glycogen storage disease type I: summary of the discussions. Eur J Pediatr. 1993;152 Suppl 1:87–8.
4. Coleman RA et al. Glycogen debranching enzyme deficiency: long-term study of serum enzyme activities and clinical features. J Inherit Metab Dis. 1992;15(6):869–81.
5. Smit GP. The long-term outcome of patients with glycogen storage disease type Ia. Eur J Pediatr. 1993;152 Suppl 1:S52–5.
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