位置：成果数据库 > 期刊 > 期刊详情页
A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease
  • ISSN号：0304-3940
  • 期刊名称：Neuroscience Letters
  • 时间：0
  • 页码：198-201
  • 相关项目：PINK1蛋白与BAG5蛋白的相互作用在帕金森病发病机制中的作用研究
作者： Wang, Lei|Guo, Ji-feng|Nie, Li-luo|Xu, Qian|Zuo, Xing|Sun, Qi-ying|Yan, Xin-xiang|Tang, Bei-sha|
同期刊论文项目
PINK1蛋白与BAG5蛋白的相互作用在帕金森病发病机制中的作用研究
期刊论文 29
同项目期刊论文
PITX3 gene polymorphism is associated with Parkinson’s disease in Chinese population
Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease
Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese populat
Clinical features and [C-11]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive earl
Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset park
A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease
BAG5蛋白与帕金森病相关蛋白Parkin的相互作用
PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort
中国汉族人群早发性帕金森综合征DJ-1基因突变分析
Direct Interaction Between Two Parkinson-related Protein Parkin and PINK1
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal d
Lower serum UA levels in Parkinson's disease patients in the Chinese population
Analysis of PLA2G6 gene mutation in sporadic early-onset parkinsonism patients from Chinese populati
Variant in the 3' region of SNCA associated with Parkinson's disease and serum alpha-synuclein level
脑内铁沉积神经变性病临床特点及PLA2G6基因突变研究
帕金森病相关蛋白Parkin与PINK1的相互作用研究
DJ-1基因L10P突变导致氧化应激和线粒体功能障碍（英文）
早发性帕金森综合征的PINK1基因变异分析（英文）
LINGO1基因多态性与多系统萎缩相关性研究
中国汉族帕金森病人microRNA-7变异分析
中国南方汉族散发早发性帕金森综合征的parkin基因突变分析