Glycogenosis Type II


Enzyme Replacement Therapy Glycogen Storage Disease Fanconi Syndrome Glycogen Storage Disease Type Alpha Glucosidase 
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  1. Hirschhorn R, and Reuser A (2001) Glycogen storage disease type II: acid α-glucosidase (acid maltase) deficiency. In: The metabolic and molecular bases of inherited diseases. (Scriver C, Beaudet A, Valle D, and Sly W, eds). New York: McGraw-Hill, pp 3389Google Scholar
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