Linking a genome-wide association study signal to aLRRK2coding variant in Parkinson's disease-Reference-Cited by-同舟云学术

Linking a genome-wide association study signal to aLRRK2coding variant in Parkinson's disease

Published:2015-12-21 Issue:4 Volume:31 Page:484-487
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Foo Jia Nee¹,Chung Sun Ju²,Tan Louis C.³,Liany Herty¹,Ryu Ho-Sung²,Hong Myunghee⁴,Koh Tat Hung¹,Irwan Ishak D.¹,Au Wing-Lok³,Prakash Kumar-M.³,Aung Tin⁵⁶,Cheng Ching-Yu⁵⁶⁷,Chong Siow-Ann⁸,Khor Chiea Chuen¹⁵⁹,Lee Jimmy⁷⁸,Tai E-Shyong¹⁰¹¹,Vithana Eranga N.⁵⁶⁷,Wong Tien-Yin⁵⁶⁷,Song Kyuyoung⁴,Liu Jianjun¹¹¹,Tan Eng-King³⁷

Affiliation:

1. Human Genetics, Genome Institute of Singapore, A*STAR; Singapore

2. Department of Neurology, Asan Medical Center; University of Ulsan College of Medicine; Seoul Korea

3. Department of Neurology, Singapore General Hospital; National Neuroscience Institute; Singapore

4. Department of Biochemistry and Molecular Biology; University of Ulsan College of Medicine; Seoul Korea

5. Singapore Eye Research Institute; Singapore

6. Department of Ophthalmology, Yong Loo Lin School of Medicine; National University of Singapore; Singapore

7. Duke-National University of Singapore Graduate Medical School; Singapore

8. Institute of Mental Health; Singapore

9. Department of Biochemistry, Yong Loo Lin School of Medicine; National University of Singapore, Singapore; Singapore

10. Department of Medicine, Yong Loo Lin School of Medicine; National University of Singapore, National University Health System; Singapore

11. Saw Swee Hock School of Public Health; National University of Singapore, National University Health System; Singapore

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.26495/fullpdf

Reference12 articles.

1. Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study;Tan;Hum Mutat,2010

2. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisán-Ruíz;Neuron,2004

3. Mutations in LRRK2 increase phosphorylation of peroxiredoxin 3 exacerbating oxidative stress-induced neuronal death;Angeles;Hum Mutat,2011

4. Parkin protects against LRRK2 G2019S mutant-induced dopaminergic neurodegeneration in Drosophila;Ng;J Neurosci,2009

5. Deletion of the WD40 domain of LRRK2 in Zebrafish causes Parkinsonism-like loss of neurons and locomotive defect;Sheng;PLoS Genet,2010

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