Partial phenotypic correction and immune
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Gaëlle Douillard-Guilloux; Emmanuel Richard; Lionel Batista; Catherine Caillaud
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Article
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2009
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John Wiley and Sons
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English
⚖ 472 KB
👁 1 views
## Abstract ## Background Glycogen storage disease type II (GSDII) or Pompe disease is an inherited disease of glycogen metabolism caused by a lack of functional lysosomal acid α‐glucosidase (GAA). Affected individuals store glycogen in lysosomes resulting in fatal hypertrophic cardiomyopathy and