Impaired cellular bioenergetics caused by GBA1 depletion sensitizes neurons to calcium overload

Heterozygous mutations of the lysosomal enzyme glucocerebrosidase (GBA1) represent the major genetic risk for Parkinson’s disease (PD), while homozygous GBA1 mutations cause Gaucher disease, a lysosomal storage disorder, which may involve severe neurodegeneration. We have previously demonstrated imp...

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Detalles Bibliográficos
Autores principales: Plotegher, Nicoletta, Perocheau, Dany, Ferrazza, Ruggero, Massaro, Giulia, Bhosale, Gauri, Zambon, Federico, Rahim, Ahad A., Guella, Graziano, Waddington, Simon N., Szabadkai, Gyorgy, Duchen, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206133/
https://www.ncbi.nlm.nih.gov/pubmed/31685979
http://dx.doi.org/10.1038/s41418-019-0442-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206133/
https://www.ncbi.nlm.nih.gov/pubmed/31685979
http://dx.doi.org/10.1038/s41418-019-0442-2

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