Lrrk

Some articles on lrrk:

LRRK2 - Clinical Significance
... The Gly2019Ser mutation in LRRK2 is a relatively common cause of familial Parkinson's Disease in Caucasians ... It may also cause sporadic Parkinson's Disease ...
LRRK2 - Function
... LRRK2 interacts with the C-terminal R2 RING finger domain of parkin, and parkin interacted with the COR domain of LRRK2 ... Expression of mutant LRRK2 induced apoptotic cell death in neuroblastoma cells and in mouse cortical neurons ...