Article

Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson’s disease at Chr16q11.2 and on the MAPT H1 allele

2020-01-07

Abstract excerpt

<h4>ABSTRACT</h4> Parkinson’s disease (PD) is a common incurable neurodegenerative disease. The identification of genetic variants via genome-wide association studies (GWAS) has considerably advanced our understanding of the PD genetic risk. Understanding the functional significance of the risk loci is now a critical step towards translating these genetic advances into an enhanced biological understanding of the...

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Literature Corpus work: ef06d0ee-b024-588f-8a6b-82a3386f46c4
DOI: 10.1101/2020.01.06.896241

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