Synaptic Function and Dysfunction in Lysosomal Storage Diseases

Lysosomal storage diseases (LSDs) with neurological involvement are inherited genetic diseases of the metabolism characterized by lysosomal dysfunction and the accumulation of undegraded substrates altering glial and neuronal function. Often, patients with neurological manifestations present with da...

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Detalles Bibliográficos
Autores principales: Rebiai, Rima, Givogri, Maria I., Gowrishankar, Swetha, Cologna, Stephania M., Alford, Simon T., Bongarzone, Ernesto R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cellular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7978225/
https://www.ncbi.nlm.nih.gov/pubmed/33746713
http://dx.doi.org/10.3389/fncel.2021.619777

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7978225/
https://www.ncbi.nlm.nih.gov/pubmed/33746713
http://dx.doi.org/10.3389/fncel.2021.619777

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