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Uptake of moss‐derived human recombinant GAA in Gaa (−/−) mice
Pompe disease, an autosomal recessive lysosomal storage disorder, is caused by deficiency of lysosomal acid alpha‐glucosidase (GAA). On cellular level, there is lysosomal‐bound and free accumulation of glycogen and subsequent damage of organelles and organs. The most severe affected tissues are skel...
में बचाया:
| में प्रकाशित: | JIMD Rep |
|---|---|
| मुख्य लेखकों: | , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
John Wiley & Sons, Inc.
2021
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8100399/ https://ncbi.nlm.nih.gov/pubmed/33977033 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jmd2.12203 |
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