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The Roles of PINK1, Parkin and Mitochondrial Fidelity in Parkinson's Disease

Understanding the function of genes mutated in hereditary forms of Parkinson's disease yields insight into disease etiology and reveals new pathways in cell biology. Although mutations or variants in many genes increase the susceptibility to Parkinson's disease, only a handful of monogenic...

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Bibliografske podrobnosti
izdano v:Neuron
Main Authors: Pickrell, Alicia M., Youle, Richard J.
Format: Artigo
Jezik:Inglês
Izdano: 2015
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4764997/
https://ncbi.nlm.nih.gov/pubmed/25611507
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2014.12.007
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