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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Detalles Bibliográficos
Autores principales: McCall, Angela L., Dhindsa, Justin S., Bailey, Aidan M., Pucci, Logan A., Strickland, Laura M., ElMallah, Mai K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Society of Smooth Muscle Research 2021
Materias:
Original
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053439/
https://www.ncbi.nlm.nih.gov/pubmed/33883348
http://dx.doi.org/10.1540/jsmr.57.8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053439/
https://www.ncbi.nlm.nih.gov/pubmed/33883348
http://dx.doi.org/10.1540/jsmr.57.8

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