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Literature summary for 3.2.1.117 extracted from
- Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations. (2009), J Hum Genet, , .
Organism
| Organism | UniProt | Comment | Textmining |
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Release 2023.1 (January 2023)
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