| Literature DB >> 24455477 |
David A Wenger1, Paola Luzi1, Mohammad A Rafi1.
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.Entities:
Keywords: LSDs; Lysosomal storage diseases; Psychosine; SAPs; Saposins; Sphingolipid activator proteins
Year: 2013 PMID: 24455477 PMCID: PMC3892733 DOI: 10.5681/bi.2013.029
Source DB: PubMed Journal: Bioimpacts ISSN: 2228-5652