Lysosomal positioning diseases: beyond substrate storage

Lysosomal storage diseases (LSDs) comprise a group of inherited monogenic disorders characterized by lysosomal dysfunctions due to undegraded substrate accumulation. They are caused by a deficiency in specific lysosomal hydrolases involved in cellular catabolism, or non-enzymatic proteins essential...

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Detalles Bibliográficos
Autores principales: Scerra, Gianluca, De Pasquale, Valeria, Scarcella, Melania, Caporaso, Maria Gabriella, Pavone, Luigi Michele, D'Agostino, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597170/
https://www.ncbi.nlm.nih.gov/pubmed/36285443
http://dx.doi.org/10.1098/rsob.220155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597170/
https://www.ncbi.nlm.nih.gov/pubmed/36285443
http://dx.doi.org/10.1098/rsob.220155

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