Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons
| Autor: | Schapansky, Jason a, Khasnavis, Saurabh a, DeAndrade, Mark P. a, Nardozzi, Jonathan D. a, Falkson, Samuel R. a, Boyd, Justin D. a, Sanderson, John B. a, Bartels, Tim a, Melrose, Heather L. b, LaVoie, Matthew J. a, ⁎ |
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| Zdroj: | In Neurobiology of Disease March 2018 111:26-35 |
| Databáze: | ScienceDirect |
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