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    {
        "title": "Glutamine-specific N-terminal amidase, a component of the N-end rule pathway.",
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        "authors": "Wang H, Piatkov KI, Brower CS, Varshavsky A",
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        "title": "Glycogen storage disease type IIIa: first report of a causative missense mutation (G1448R) of the glycogen debranching enzyme gene found in a homozygous patient.",
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        "authors": "Okubo M, Kanda F, Horinishi A, Takahashi K, Okuda S, Chihara K, Murase T",
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                                "name": "glycogen storage disease III",
                                "description": "Glycogen debranching enzyme (GDE) deficiency, or glycogen storage disease type 3 (GSD 3), is a form of glycogen storage disease characterized by severe muscle weakness and hepatopathy."
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                            {
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        "title": "Compound heterozygous patient with glycogen storage disease type III: identification of two novel AGL mutations, a donor splice site mutation of Chinese origin and a 1-bp deletion of Japanese origin.",
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        "title": "Molecular cloning and nucleotide sequence of cDNA encoding human muscle glycogen debranching enzyme.",
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        "title": "Spectrum of amyloglucosidase mutations in Asian Indian patients with Glycogen storage disease type III.",
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