Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort

被引：2
|
作者：
Li, Chunyu [1 ]
Lin, Junyu [1 ]
Jiang, Qirui [1 ]
Yang, Tianmi [1 ]
Xiao, Yi [1 ]
Huang, Jingxuan [1 ]
Hou, Yanbing [1 ]
Wei, Qianqian [1 ]
Wang, Shichan [1 ]
Zheng, Xiaoting [1 ]
Ou, Ruwei [1 ]
Liu, Kuncheng [1 ]
Chen, Xueping [1 ]
Song, Wei [1 ]
Zhao, Bi [1 ]
Shang, Huifang [1 ]
机构：
[1] Sichuan Univ, West China Hosp, Dept Neurol, Lab Neurodegenerat Disorders,Rare Dis Ctr, Chengdu, Peoples R China
来源：
MOVEMENT DISORDERS | 2023年 / 38卷 / 04期
基金：
中国国家自然科学基金;
关键词：
D O I：
10.1002/mds.29372
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：708 / 709
页数：2
相关论文
共 50 条
  • [31] Rare variants in dementia genes and Parkinson's disease
    Iqbal, Zafar
    Pihlstrom, Lasse
    Rengmark, Aina
    Henriksen, Sandra Pilar
    Linder, Jan
    Forsgren, Lars
    Toft, Mathias
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2016, 24 (12) : 1661 - 1662
  • [32] Rare variants in dementia genes and Parkinson’s disease
    Zafar Iqbal
    Lasse Pihlstrøm
    Aina Rengmark
    Sandra Pilar Henriksen
    Jan Linder
    Lars Forsgren
    Mathias Toft
    European Journal of Human Genetics, 2016, 24 : 1661 - 1662
  • [33] Lack of Association Between DNMT3B Polymorphisms and Sporadic Parkinson's Disease in a Han Chinese Population
    Hong Pan
    Jun-Yi Shen
    Juan-Juan Du
    Shi-Shuang Cui
    Jin Liu
    Yi-Qi Lin
    Yi-Xi He
    Yang Fu
    Chao Gao
    Gen Li
    Sheng-Di Chen
    Jian-Fang Ma
    Neuroscience Bulletin, 2018, (05) : 867 - 869
  • [34] Lack of Association Between DNMT3B Polymorphisms and Sporadic Parkinson's Disease in a Han Chinese Population
    Pan, Hong
    Shen, Jun-Yi
    Du, Juan-Juan
    Cui, Shi-Shuang
    Liu, Jin
    Lin, Yi-Qi
    He, Yi-Xi
    Fu, Yang
    Gao, Chao
    Li, Gen
    Chen, Sheng-Di
    Ma, Jian-Fang
    NEUROSCIENCE BULLETIN, 2018, 34 (05) : 867 - 869
  • [35] Lack of Association Between DNMT3B Polymorphisms and Sporadic Parkinson’s Disease in a Han Chinese Population
    Hong Pan
    Jun-Yi Shen
    Juan-Juan Du
    Shi-Shuang Cui
    Jin Liu
    Yi-Qi Lin
    Yi-Xi He
    Yang Fu
    Chao Gao
    Gen Li
    Sheng-Di Chen
    Jian-Fang Ma
    Neuroscience Bulletin, 2018, 34 : 867 - 869
  • [36] Rare UQCRC1 variants in Chinese patients with Early Onset Parkinson's Disease
    Gu, X. J.
    Hou, Y. B.
    Chen, Y. P.
    Ou, R. W.
    Shang, H. F.
    MOVEMENT DISORDERS, 2021, 36 : S309 - S310
  • [37] Lack of Association between MC1R Variants and Parkinson Disease in European Descent Reply
    Tell-Marti, Gemma
    Puig-Butille, Joan Anton
    Potrony, Miriam
    Badenas, Celia
    Mila, Montserrat
    Malvehy, Josep
    Marti, Maria Jose
    Ezquerra, Mario
    Fernandez-Santiago, Ruben
    Puig, Susana
    ANNALS OF NEUROLOGY, 2016, 79 (05) : 868 - 868
  • [38] The lack of association between ubiquinol-cytochrome c reductase core protein I (UQCRC1) variants and Parkinson's disease in an eastern Chinese population
    Lin, Zhi-Hao
    Zheng, Ran
    Ruan, Yang
    Gao, Ting
    Jin, Chong-Yao
    Xue, Nai-Jia
    Dong, Jia-Xian
    Yan, Ya-Ping
    Tian, Jun
    Pu, Jia-Li
    Zhang, Bao-Rong
    CNS NEUROSCIENCE & THERAPEUTICS, 2020, 26 (09) : 990 - 992
  • [39] Reply: PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population
    Oji, Yutaka
    Hatano, Taku
    Funayama, Manabu
    Hattori, Nobutaka
    BRAIN, 2021, 144 (03)
  • [40] Relationship between variants of 17 newly loci and Parkinson's disease in a Chinese population
    Chen, Xiang
    Xiao, Yousheng
    Guo, Wenyuan
    Zhou, Miaomiao
    Huang, Shuxuan
    Mo, Mingshu
    Li, Zhe
    Li, Guihua
    Liu, Hanqun
    Peng, Guoyou
    Wu, Zhuohua
    Wu, Yijuan
    Yang, Chaohao
    Pei, Zhong
    Chen, Chaojun
    Xu, Pingyi
    NEUROBIOLOGY OF AGING, 2019, 73 : 230.e1 - 230.e4
12345