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Neurobiology of Disease|December 17, 2017
Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neuronsJason Schapansky, Saurabh Khasnavis, Mark P DeAndrade, et al.
Neurobiology of Disease|December 17, 2017
Toxic properties of microsome-associated alpha-synuclein species in mouse primary neuronsEmanuela Colla, Giulia Panattoni, Alessio Ricci, et al.
Neurobiology of Disease|May 19, 2022
FTD-associated mutations in Tau result in a combination of dominant and recessive phenotypesAlexander D Law, Marlène Cassar, Dani M Long, et al.
Neurobiology of Disease|May 19, 2022
Targeting the MGBA with -biotics in epilepsy: New insights from preclinical and clinical studiesAntonella Riva, Elisa Pozzati, Mattia Grasso, et al.
Neurobiology of Disease|May 23, 2022
Altered retinal structure and function in Spinocerebellar ataxia type 3Vasileios Toulis, Ricardo Casaroli-Marano, Anna Camós-Carreras, et al.
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