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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Bibliografiske detaljer
Udgivet i:EMBO J
Main Authors: Ikonen, E, Julkunen, I, Tollersrud, O K, Kalkkinen, N, Peltonen, L
Format: Artigo
Sprog:Inglês
Udgivet: Nature Publishing Group 1993
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC413205/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8428587/
https://ncbi.nlm.nih.govhttps://doi.org/10.1002/j.1460-2075.1993.tb05656.x
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