Additional file 6: Figure S6. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation

Rab8a protein levels and pericentrosomal/centrosomal accumulation of phosphorylated Rab8a in lymphoblasts from control and G2019S mutant LRRK2 PD patients. (DOCX 636 kb)