RAB7L1-Mediated Relocalization of LRRK2 to the Golgi Complex Causes Centrosomal Deficits via RAB8A
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DOI: 10.3389/fnmol.2018.00417
Abstract: Mutations in the LRRK2 gene cause autosomal-dominant Parkinson’s disease (PD), and both LRRK2 as well as RAB7L1 have been implicated in increased susceptibility to idiopathic PD. RAB7L1 has been shown to increase membrane-association and kinase… read more here.
Keywords: lrrk2 golgi; rab8a; rab7l1; lrrk2 ... See more keywords