ATP13A2/PARK9 Deficiency Neither Cause Lysosomal Impairment Nor Alter α-Synuclein Metabolism in SH-SY5Y Cells

Parkinson's disease is a multifactorial disorder with several genes linked to the familial types of the disease. ATP13A2 is one of those genes and encode for a transmembrane protein localized in lysosomes and late endosomes. Previous studies suggested the roles of this protein in lysosomal func...

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Detalles Bibliográficos
Autores principales: Bae, Eun-Jin, Lee, Cheolsoon, Lee, He-Jin, Kim, Seokjoong, Lee, Seung-Jae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276807/
https://www.ncbi.nlm.nih.gov/pubmed/25548536
http://dx.doi.org/10.5607/en.2014.23.4.365

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276807/
https://www.ncbi.nlm.nih.gov/pubmed/25548536
http://dx.doi.org/10.5607/en.2014.23.4.365

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