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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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Front Cell Neurosci
Prif Awduron: Rebiai, Rima, Givogri, Maria I., Gowrishankar, Swetha, Cologna, Stephania M., Alford, Simon T., Bongarzone, Ernesto R.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2021
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7978225/
https://ncbi.nlm.nih.gov/pubmed/33746713
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2021.619777
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