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Parkinsonisms and Glucocerebrosidase Deficiency: A Comprehensive Review for Molecular and Cellular Mechanism of Glucocerebrosidase Deficiency

In the last years, lysosomal storage diseases appear as a bridge of knowledge between rare genetic inborn metabolic disorders and neurodegenerative diseases such as Parkinson’s disease (PD) or frontotemporal dementia. Epidemiological studies helped promote research in the field that continues to imp...

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Detalhes bibliográficos
Publicado no:Brain Sci
Main Authors: Gatto, Emilia M., Da Prat, Gustavo, Etcheverry, Jose Luis, Drelichman, Guillermo, Cesarini, Martin
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6406566/
https://ncbi.nlm.nih.gov/pubmed/30717266
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/brainsci9020030
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