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VPS35 pathogenic mutations confer no dominant toxicity but partial loss of function in Drosophila and genetically interact with parkin

Mutations in VPS35 (PARK17) cause autosomal dominant, late onset Parkinson's disease (PD). VPS35 forms a core component of the retromer complex that mediates the retrieval of membrane proteins from endosomes back to either the Golgi or plasma membrane. While aberrant endosomal protein sorting h...

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Bibliografiske detaljer
Udgivet i:Hum Mol Genet
Main Authors: Malik, Bilal R., Godena, Vinay K., Whitworth, Alexander J.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2015
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4599670/
https://ncbi.nlm.nih.gov/pubmed/26251041
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv322
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