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Astrocytes and Lysosomal Storage Diseases

Lysosomal storage diseases (LSDs) encompass a wide range of disorders characterized by inborn errors of lysosomal function. The majority of LSDs result from genetic defects in lysosomal enzymes, although some arise from mutations in lysosomal proteins that lack known enzymatic activity. Neuropatholo...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Neuroscience
Prif Awduron: Rama Rao, Kakulavarapu V., Kielian, Tammy
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2015
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4664580/
https://ncbi.nlm.nih.gov/pubmed/26037807
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2015.05.061
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