Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV

By Lee Yi-Ching   Chang Chia-Jung   Bali Deeksha   Chen Yuan-Tsong   Yan Yu-Ting  

Human Molecular Genetics, Vol. 20, Iss. 3, 2011-02 ,pp. : 455-465

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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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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Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease

By Reuser A.J.J.  

Human Molecular Genetics, Vol. 7, Iss. 1, 1998-01 ,pp. : 53-62

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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