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Glycogen accumulation in smooth muscle of a Pompe disease mouse model
Pompe disease is a lysosomal storage disease caused by mutations within the GAA gene, which encodes acid α-glucosidase (GAA)—an enzyme necessary for lysosomal glycogen degradation. A lack of GAA results in an accumulation of glycogen in cardiac and skeletal muscle, as well as in motor neurons. The o...
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| Publicado no: | J Smooth Muscle Res |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Japan Society of Smooth Muscle Research
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8053439/ https://ncbi.nlm.nih.gov/pubmed/33883348 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1540/jsmr.57.8 |
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