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Dysregulation of Multiple Facets of Glycogen Metabolism in a Murine Model of Pompe Disease
Pompe disease, also known as glycogen storage disease (GSD) type II, is caused by deficiency of lysosomal acid α-glucosidase (GAA). The resulting glycogen accumulation causes a spectrum of disease severity ranging from a rapidly progressive course that is typically fatal by 1 to 2 years of age to a...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3572993/ https://ncbi.nlm.nih.gov/pubmed/23457523 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0056181 |
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