Ambroxol improves lysosomal biochemistry in glucocerebrosidase mutation-linked Parkinson disease cells

Gaucher disease is caused by mutations in the glucocerebrosidase gene, which encodes the lysosomal hydrolase glucosylceramidase. Patients with Gaucher disease and heterozygous glucocerebrosidase mutation carriers are at increased risk of developing Parkinson’s disease. Indeed, glucocerebrosidase mut...

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Detalles Bibliográficos
Autores principales: McNeill, Alisdair, Magalhaes, Joana, Shen, Chengguo, Chau, Kai-Yin, Hughes, Derralyn, Mehta, Atul, Foltynie, Tom, Cooper, J. Mark, Abramov, Andrey Y., Gegg, Matthew, Schapira, Anthony H.V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999713/
https://www.ncbi.nlm.nih.gov/pubmed/24574503
http://dx.doi.org/10.1093/brain/awu020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999713/
https://www.ncbi.nlm.nih.gov/pubmed/24574503
http://dx.doi.org/10.1093/brain/awu020

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