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Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons. [electronic resource] by
- 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
Producer: 20190617
In:
Neurobiology of disease vol. 111
Availability: No items available.
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4367.
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Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy. [electronic resource] by
- Shahnawaz, Mohammad
- Mukherjee, Abhisek
- Pritzkow, Sandra
- Mendez, Nicolas
- Rabadia, Prakruti
- Liu, Xiangan
- Hu, Bo
- Schmeichel, Ann
- Singer, Wolfgang
- Wu, Gang
- Tsai, Ah-Lim
- Shirani, Hamid
- Nilsson, K Peter R
- Low, Phillip A
- Soto, Claudio
Producer: 20200420
In:
Nature vol. 578
Availability: No items available.
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