Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration

Mutations in the vacuolar protein sorting 35 homolog (VPS35) gene at the PARK17 locus, encoding a key component of the retromer complex, were recently identified as a new cause of late-onset, autosomal dominant Parkinson's disease (PD). Here we explore the pathogenic consequences of PD-associat...

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Main Authors: Tsika, Elpida, Glauser, Liliane, Moser, Roger, Fiser, Aris, Daniel, Guillaume, Sheerin, Una-Marie, Lees, Andrew, Troncoso, Juan C., Lewis, Patrick A., Bandopadhyay, Rina, Schneider, Bernard L., Moore, Darren J.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4119414/
https://ncbi.nlm.nih.gov/pubmed/24740878
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu178
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