K.Y. Puong

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients

Eng‐King Tan, Hui Shen, Louis C.S. Tan et al. · Neuroscience Letters · 2005 · 152 citations

G2019s Lrrk2 Mutation, Parkinson Disease, Pathology +4

Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort

Eng‐King Tan, Yongxiang Zhao, K.Y. Puong et al. · Neurology · 2004 · 75 citations

Genetics, Genetic Epidemiology, Human Polymorphism +16

Analysis of <i>LRRK2</i> functional domains in nondominant Parkinson disease

Lisa Skipper, Hui Shen, E. Chua et al. · Neurology · 2005 · 75 citations

Neurodegenerative Diseases, Signal Transduction, Molecular Neuroscience +13

Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease

S.W. Lim, Yi Zhao, E. Chua et al. · Neuroscience Letters · 2006 · 28 citations

Genetic Analysis, Neurodegenerative Diseases, Idiopathic Parkinson +8