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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Dades bibliogràfiques
Publicat a:Dis Model Mech
Autors principals: 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
Idioma:Inglês
Publicat: The Company of Biologists Ltd 2017
Matèries:
Research Article
Accés en línia: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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