Glycogen storage in multiple muscles of
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Fang Xu; Enyu Ding; Felicia Migone; Delila Serra; Ayn Schneider; Yuan-Tsong Chen
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Article
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2005
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John Wiley and Sons
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English
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Background Glycogen storage disease II (GSD-II) is an autosomal recessive lysosomal storage disease, due to acid-alpha-glucosidase (GAA) deficiency. The disease is characterized by massive glycogen accumulation in the cardiac and skeletal muscles. There is early onset (infantile, also known as Pompe