Glycogenosome accumulation in the arrector pili muscle in Pompe disease

BACKGROUND: Glycogenosis type II or Pompe disease is an autosomal-recessive lysosomal storage disease due to mutations in the gene encoding acid alpha-glucosidase (GAA), an enzyme required for lysosomal glycogen degradation. The disease predominantly affects the skeletal and respiratory muscles but...

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Detalles Bibliográficos
Autores principales: Katona, Istvan, Weis, Joachim, Hanisch, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922310/
https://www.ncbi.nlm.nih.gov/pubmed/24495340
http://dx.doi.org/10.1186/1750-1172-9-17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922310/
https://www.ncbi.nlm.nih.gov/pubmed/24495340
http://dx.doi.org/10.1186/1750-1172-9-17

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