Adenovirus-mediated transfer of the acid α-glucosidase gene into fibroblasts, myoblasts and myotubes from patients with glycogen storage disease type II leads to high level expression of enzyme and corrects glycogen accumulation

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Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1695-1702

Oxford University Press

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Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease

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Human acid α -glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II

By Bijvoet Agnes G. A.  

Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2145-2153

Oxford University Press

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Identification of a mutation in liver glycogen phosphorylase in glycogen storage disease type VI

By Chang S.  

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Evidence for a Founder Effect in Sicilian Patients with Glycogen Storage Disease Type II

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