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From Acid Alpha-Glucosidase Deficiency to Autophagy: Understanding the Bases of POMPE Disease
Pompe disease (PD) is caused by mutations in the GAA gene, which encodes the lysosomal enzyme acid alpha-glucosidase, causing lysosomal glycogen accumulation, mainly in muscular tissue. Autophagic buildup is considered the main factor affecting skeletal muscle, although other processes are also invo...
Autores principales: | Sánchez-Porras, Valentina, Guevara-Morales, Johana Maria, Echeverri-Peña, Olga Yaneth |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419125/ https://www.ncbi.nlm.nih.gov/pubmed/37569856 http://dx.doi.org/10.3390/ijms241512481 |
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