VPS35, the Retromer Complex and Parkinson’s Disease

Mutations in the vacuolar protein sorting 35 ortholog (VPS35) gene encoding a core component of the retromer complex, have recently emerged as a new cause of late-onset, autosomal dominant familial Parkinson’s disease (PD). A single missense mutation, AspD620Asn (D620N), has so far been unambiguousl...

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Detalles Bibliográficos
Autores principales: Williams, Erin T., Chen, Xi, Moore, Darren J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438477/
https://www.ncbi.nlm.nih.gov/pubmed/28222538
http://dx.doi.org/10.3233/JPD-161020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438477/
https://www.ncbi.nlm.nih.gov/pubmed/28222538
http://dx.doi.org/10.3233/JPD-161020

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