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Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
Madero-Pérez, Jesús, Fdez, Elena, Fernández, Belén, Lara Ordóñez, Antonio J., Blanca Ramírez, Marian, Gómez-Suaga, Patricia, Waschbüsch, Dieter, Lobbestael, Evy, Baekelandt, Veerle, Nairn, Angus C., RVolume:
13
Language:
english
Journal:
Molecular Neurodegeneration
DOI:
10.1186/s13024-018-0235-y
Date:
December, 2018
File:
PDF, 12.39 MB
english, 2018