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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Neuroscience
Egile Nagusiak: Rama Rao, Kakulavarapu V., Kielian, Tammy
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2015
Gaiak:
Sarrera elektronikoa: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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