Pathogenic Parkinson’s disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation()

LRRK2 is one of the most important genetic contributors to Parkinson’s disease (PD). Point mutations in this gene cause an autosomal dominant form of PD, but to date no cellular phenotype has been consistently linked with mutations in each of the functional domains (ROC, COR and Kinase) of the prote...

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Detalles Bibliográficos
Autores principales: Manzoni, Claudia, Mamais, Adamantios, Dihanich, Sybille, McGoldrick, Phillip, Devine, Michael J., Zerle, Julia, Kara, Eleanna, Taanman, Jan-Willem, Healy, Daniel G., Marti-Masso, Jose-Felix, Schapira, Anthony H., Plun-Favreau, Helene, Tooze, Sharon, Hardy, John, Bandopadhyay, Rina, Lewis, Patrick A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3858825/
https://www.ncbi.nlm.nih.gov/pubmed/24211199
http://dx.doi.org/10.1016/j.bbrc.2013.10.159

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3858825/
https://www.ncbi.nlm.nih.gov/pubmed/24211199
http://dx.doi.org/10.1016/j.bbrc.2013.10.159

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