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

By Nicolino M.P.  

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

Oxford University Press

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

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Human Heredity, Vol. 50, Iss. 6, 2000-07 ,pp. : 331-333

Karger

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Recombinant human acid α-glucosidase: high level production in mouse milk, biochemical characteristics, correction of enzyme deficiency in GSDII KO mice

By Bijvoet A.G.A.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1815-1824

Oxford University Press

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Sustained hepatic and renal glucose-6-phosphatase expression corrects glycogen storage disease type Ia in mice

By Sun M-S.  

Human Molecular Genetics, Vol. 11, Iss. 18, 2002-06 ,pp. : 2155-2164

Oxford University Press

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

By Chang S.  

Human Molecular Genetics, Vol. 7, Iss. 5, 1998-05 ,pp. : 865-870

Oxford University Press

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