Associated Papers
Absence of commonly reported leucine-rich repeat kinase 2 mutations in Eastern Indian Parkinson's disease patients.
Sanyal J et al.
Genetic Testing and Molecular Biomarkers, 2010
A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease.
Wang L et al.
Neuroscience Letters, 2010
The LRRK2 I2012T, G2019S and I2020T mutations are not common in patients with essential tremor.
Deng H et al.
Neuroscience Letters, 2006
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease.
Lu CS et al.
Parkinsonism & Related Disorders, 2005
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