Neurodegenerative Lysosomal Storage Disorders: TPC2 Comes to the Rescue!

Lysosomal storage diseases (LSDs) resulting from inherited gene mutations constitute a family of disorders that disturb lysosomal degradative function leading to abnormal storage of macromolecular substrates. In most LSDs, central nervous system (CNS) involvement is common and leads to the progressi...

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Detalles Bibliográficos
Autores principales: Prat Castro, Sandra, Kudrina, Veronika, Jaślan, Dawid, Böck, Julia, Scotto Rosato, Anna, Grimm, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496660/
https://www.ncbi.nlm.nih.gov/pubmed/36139381
http://dx.doi.org/10.3390/cells11182807

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496660/
https://www.ncbi.nlm.nih.gov/pubmed/36139381
http://dx.doi.org/10.3390/cells11182807

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