
Developed in collaboration with the Michael J Fox Foundation, this model contains a deletion of the Lrrk2 gene, encoding for the leucine-rich repeat kinase 2.
Lrrk2 mutations account for 5-6% of familial Parkinson’s dieases and 1-3% in sporadic PD. Collectively, these mutations result in the most common cause of PD, making this an important model for the study of Parkinson’s disease.