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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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Detaylı Bibliyografya
Yayımlandı:Neuron
Asıl Yazarlar: Pickrell, Alicia M., Youle, Richard J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2015
Konular:
Online Erişim: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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