Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at Chr16q11.2 and on the MAPT H1 allele (2020)

First Author: Soutar M

Attributed to: Mitochondrial and synaptic dysfunction in neurons from patients with OPA1- associated parkinsonism funded by NERC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/2020.01.06.896241

Publication URI: http://dx.doi.org/10.1101/2020.01.06.896241

Type: Preprint