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Cardiolipin promotes electron transport between ubiquinone and complex I to rescue PINK1 deficiency
PINK1 is mutated in Parkinson’s disease (PD), and mutations cause mitochondrial defects that include inefficient electron transport between complex I and ubiquinone. Neurodegeneration is also connected to changes in lipid homeostasis, but how these are related to PINK1-induced mitochondrial dysfunct...
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| Gepubliceerd in: | J Cell Biol |
|---|---|
| Hoofdauteurs: | , , , , , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The Rockefeller University Press
2017
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5346965/ https://ncbi.nlm.nih.gov/pubmed/28137779 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201511044 |
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