glycogen storage disease due to glycogen branching enzyme deficiency
glycogen storage disease due to glycogen branching enzyme deficiency
Explore linked clinical trials. Standard reference: MONDO:00092921 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| GBE Deficiency (GSD IV and APBD) Natural History Study | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, adult polyglucosan body disease, disorder of glycogen metabolism, glycogen storage disease due to glycogen branching enzyme deficiency, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, metabolic disease | Recruiting | Not stated | 2026-05-05 | NCT02683512 |