Associated Papers
G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization.
Papkovskaia TD et al.
Human Molecular Genetics, 2012
Mechanistic insight into the dominant mode of the Parkinson's disease-associated G2019S LRRK2 mutation.
Luzón-Toro B et al.
Human Molecular Genetics, 2007
Analysis of LRRK 2 G 2019 S and I 2020 T mutations in Parkinson's disease.
Bialecka M et al.
Neuroscience Letters, 2005
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
Tan EK et al.
Neuroscience Letters, 2005
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