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New therapeutic options for invasive fungal diseases

✍ Scribed by Carina A Rodriguez; Christian C Patrick


Book ID
117833204
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
79 KB
Volume
12
Category
Article
ISSN
1045-1870

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## Abstract Glycogen storage disease type II or Pompe disease (GSD II, MIM 232300) is a rare inherited metabolic myopathy caused by a deficiency of lysosomal acid α‐glucosidase or acid maltase (GAA; EC 3.2.1.20), resulting in a massive lysosomal glycogen accumulation in cardiac and skeletal muscles