Characterization of Drosophila Saposin-related mutants as a model for lysosomal sphingolipid storage diseases

Sphingolipidoses are inherited diseases belonging to the class of lysosomal storage diseases (LSDs), which are characterized by the accumulation of indigestible material in the lysosome caused by specific defects in the lysosomal degradation machinery. While some LSDs can be efficiently treated by e...

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Udgivet i:Dis Model Mech
Main Authors: Sellin, Julia, Schulze, Heike, Paradis, Marie, Gosejacob, Dominic, Papan, Cyrus, Shevchenko, Andrej, Psathaki, Olympia Ekaterina, Paululat, Achim, Thielisch, Melanie, Sandhoff, Konrad, Hoch, Michael
Format: Artigo
Sprog:Inglês
Udgivet: The Company of Biologists Ltd 2017
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5483003/
https://ncbi.nlm.nih.gov/pubmed/28389479
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.027953
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