A. Wenger, David and Luzi, Paola (2014) Lysosomal Storage Diseases: Heterogeneous Group of Disorders. BioImpacts.
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Abstract
The name of lysosomal storage diseases stems from the fact that in this category of disorders specific undegraded materials are stored in the lysosomes. This is usually caused by a lysosomal enzyme deficiency and leads to a cascade of pathological outcomes. Apart from deficiency of lysosomal enzymes, lysosomal storage diseases also include deficiencies in proteins necessary for enzyme functioning, proteins needed for post-translational modification of these enzymes and proteins required for export of certain compounds from the lysosomes.
Item Type: | Article |
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Subjects: | Apsci Archives > Medical Science |
Depositing User: | Unnamed user with email support@apsciarchives.com |
Date Deposited: | 08 Apr 2023 06:37 |
Last Modified: | 05 Mar 2024 04:04 |
URI: | http://eprints.go2submission.com/id/eprint/615 |