Genotypic and phenotypic features of 39 Chinese patients with glycogen storage diseases type I, VI, and IX

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Genotype–phenotype spectrum and clinical outcomes of glycogen storage disease type I: A 15-year experience at Vietnam National Children's Hospital2026
2. 2Unraveling the Genetic Basis of Glycogen Storage Diseases through Exome Sequencing: A Study in Pediatric Patients2026
3. 3Clinical and molecular characterization of hepatic glycogen storage disease in Saudi Arabia2025
4. 4Clinical features and rare complications in 132 patients with hepatic glycogenosis2025
5. 5A case study of a liver transplant-treated patient with glycogen storage disease type Ia presenting with multiple inflammatory hepatic adenomas: an analysis of clinicopathologic and genetic data2024