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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Detalles Bibliográficos
Autores principales: Gatto, Emilia M., Da Prat, Gustavo, Etcheverry, Jose Luis, Drelichman, Guillermo, Cesarini, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406566/
https://www.ncbi.nlm.nih.gov/pubmed/30717266
http://dx.doi.org/10.3390/brainsci9020030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406566/
https://www.ncbi.nlm.nih.gov/pubmed/30717266
http://dx.doi.org/10.3390/brainsci9020030

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