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                                       Details for article 7 of 15 found articles
 
 
  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
Author: Schapansky, Jason
Khasnavis, Saurabh
DeAndrade, Mark P.
Nardozzi, Jonathan D.
Falkson, Samuel R.
Boyd, Justin D.
Sanderson, John B.
Bartels, Tim
Melrose, Heather L.
LaVoie, Matthew J.
Appeared in: Neurobiology of disease
Paging: Volume 111 (2018) nr. C pages 26-35
Year: 2018
Contents:
Publisher: Elsevier Inc.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 7 of 15 found articles
 
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