Učitavanje...
Lysosomal aspartylglucosaminidase is processed to the active subunit complex in the endoplasmic reticulum.
Aspartylglucosaminidase (AGA) is a lysosomal enzyme, the deficiency of which leads to a human storage disease, aspartylglucosaminuria (AGU). Although numerous mutations have been identified in AGU patients, elucidation of the molecular pathogenesis of the disease has been hampered by the missing inf...
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| Glavni autori: | , , , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
1993
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC413205/ https://ncbi.nlm.nih.gov/pubmed/8428587 |
| Oznake: |
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