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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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Detalhes bibliográficos
Publicado no:Neuron
Main Authors: Pickrell, Alicia M., Youle, Richard J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha: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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