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Neuroscience Letters|November 3, 2009
A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's diseaseLei Wang, Ji-feng Guo, Li-luo Nie, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 9, 2013
[Cloning and localization of A3IP -a novel protein that interacts with ataxin-3]Feng-zhen Huang, Xuan Hou, Guo Wang, et al.
Translational Neurodegeneration|December 20, 2017
Identification of Ser465 as a novel PINK1 autophosphorylation siteJi-Feng Guo, Ling-Yan Yao, Qi-Ying Sun, et al.
Cerebrovascular Diseases (Basel, Switzerland)|December 8, 2007
Study of the relationship between gene polymorphisms of paraoxonase 2 and stroke in a Chinese populationHong-Wei Xu, Ning Yuan, Zhen Zhao, et al.
The International Journal of Neuroscience|March 9, 2016
Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland populationXiang-Qian Che, Zhan-Fang Sun, Xiao Mao, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|September 8, 2019
Preliminary study of hsa-miR-626 change in the cerebrospinal fluid of Parkinson's disease patientsLi-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Neuroscience Letters|March 17, 2011
LRRK2 Pro755Leu variant in ethnic Chinese population with Parkinson's diseaseLing-Yan Yao, Ji-Feng Guo, Lei Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2010
[Establishment and application of an analytical method for PINK1 gene exon copy number]Hai-nan Zhang, Bing Liao, Li-luo Nie, et al.
Brain Research|February 2, 2019
Impaired iPLA<sub>2</sub>β activity affects iron uptake and storage without iron accumulation: An in vitro study excluding decreased iPLA<sub>2</sub>β activity as the cause of iron deposition in PLANYu-Pei Guo, Bei-Sha Tang, Hong-Li Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 5, 2005
Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegenerationYu-hu Zhang, Bei-sha Tang, Ai-ling Zhao, et al.
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