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Therapeutic approaches in glycogen storage disease type II/pompe disease
Glycogen storage disease type II (GSDII)/Pompe disease is an autosomal recessive multi-system disorder due to a deficiency of the glycogen-degrading lysosomal enzyme, acid alpha-glucosidase. Without adequate levels of alpha-glucosidase, there is a progressive accumulation of glycogen inside the lyso...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer New York
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2761605/ https://ncbi.nlm.nih.gov/pubmed/19019308 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nurt.2008.08.009 |
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