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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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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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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Glycogen Storage Disease Type II: Birth Prevalence Agrees with Predicted Genotype Frequency

By  

Public Health Genomics, Vol. 2, Iss. 2-3, 2000-03 ,pp. : 91-96

Karger

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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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