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