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- W2004653744 endingPage "150" @default.
- W2004653744 startingPage "125" @default.
- W2004653744 abstract "The glycogen storage myopathies are caused by enzyme defects in the glycogenolytic or in the glycolytic pathway affecting skeletal muscle alone or in conjunction with other tissues. The authors review recent findings in this area, including a new entity, aldolase deficiency, and the wealth of molecular genetic data that are rapidly accumulating. Despite this progress, genotype-phenotyp3 correlations are still murky in most glycogen storage myopathies." @default.
- W2004653744 created "2016-06-24" @default.
- W2004653744 creator A5001477991 @default.
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- W2004653744 date "2000-02-01" @default.
- W2004653744 modified "2023-10-13" @default.
- W2004653744 title "GLYCOGEN STORAGE MYOPATHIES" @default.
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