Molecular characterization of Egyptian patients with glycogen storage disease type IIIa

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Molecular characterization of Egyptian patients with glycogen storage disease type IIIa
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Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa
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
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