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- W945523323 abstract "Pompe disease (glyocogen storage disease type-II) is an inherited deficiency of acid α-glucosidase (GAA), a lysosomal enzyme required for glycogen breakdown. This results in accumulation of glycoge..." @default.
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- W945523323 date "2011-11-22" @default.
- W945523323 modified "2023-09-23" @default.
- W945523323 title "Abstract 15204: Modelling Pompe Glyocogen Storage Disease with Induced Pluripotent Stem Cells" @default.
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