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No clinical trials have been registered for glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form.
3 publications have been identified in PubMed for glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form. Research spans Review / Meta-Analysis (67%) and Other (33%).
Adorisio R (2025). [PMID: 40678571](https://pubmed.ncbi.nlm.nih.gov/40678571/). *Front Cardiovasc Med*. [Review / Meta-Analysis]
Ravara B (2025). [PMID: 40047227](https://pubmed.ncbi.nlm.nih.gov/40047227/). *Eur J Transl Myol*. [Other]
Mishra K (2024). [PMID: 39334863](https://pubmed.ncbi.nlm.nih.gov/39334863/). *Biomolecules*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 21, 2026, 4:55 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center