Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons

Title
Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons
Authors
Keywords
-
Journal
NEUROBIOLOGY OF DISEASE
Volume 111, Issue -, Pages 26-35
Publisher
Elsevier BV
Online
2017-12-13
DOI
10.1016/j.nbd.2017.12.005

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