Nalaganje...
Function, structure and quality of striated muscles in the lower extremities in patients with late onset Pompe Disease—an MRI study
BACKGROUND: Pompe Disease (PD) is a rare inherited metabolic myopathy, caused by lysosomal-α-glucosidase (GAA) deficiency, which leads to glycogen accumulation within the lysosomes, resulting in cellular and tissue damage. Due to the emergence of a disease modifying treatment with recombinant GAA th...
Shranjeno v:
| izdano v: | PeerJ |
|---|---|
| Main Authors: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
PeerJ Inc.
2021
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8106912/ https://ncbi.nlm.nih.gov/pubmed/33996274 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.10928 |
| Oznake: |
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