ATP13A2 G2236A variant is rare in patients with early-onset Parkinson's disease and familial Parkinson's disease from mainland China

被引：15
|
作者：
Mao, X-Y. [1 ]
Burgunder, J-M [1 ]
Zhang, Z-J [1 ,5 ]
Chang, X-L. [1 ]
Peng, R. [1 ]
Burgunder, J-M. [2 ]
Yang, Y. [3 ]
Wang, Y-C. [4 ]
Li, T. [4 ]
Zhang, Z-J [1 ,5 ]
机构：
[1] Sichuan Univ, Dept Neurol, W China Hosp, Chengdu 610041, Peoples R China
[2] Univ Bern, Dept Neurol, Bern, Switzerland
[3] Sichuan Univ, Dept Genet, W China Hosp, Chengdu 610041, Peoples R China
[4] Sichuan Univ, Dept Psychiat, W China Hosp, Chengdu 610041, Peoples R China
[5] Tianjin First Ctr Hosp, Dept Neurol, Tianjin, Peoples R China
来源：
PARKINSONISM & RELATED DISORDERS | 2010年 / 16卷 / 03期
关键词：
P-TYPE ATPASE; DEMENTIA;
D O I：
10.1016/j.parkreldis.2009.11.010
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：235 / 236
页数：2
相关论文
共 50 条
  • [1] Mutation screening of ATP13A2 in patients with early-onset Parkinson's disease and familial Parkinson's disease from mainland China
    Mao, X. Y.
    Peng, R.
    Zhang, Z. J.
    MOVEMENT DISORDERS, 2009, 24 : S149 - S149
  • [2] ATP13A2 mutation is rare in patients with early-onset or familial Parkinson's disease in Chinese population
    Lin, C. -H.
    Tan, E. -K.
    Chen, M. -L.
    Tan, L. C.
    Lim, H. -Q.
    Chen, G. S.
    Wu, R. -M.
    MOVEMENT DISORDERS, 2009, 24 : S409 - S409
  • [3] ATP13A2 Variants in Early-Onset Parkinson's Disease Patients and Controls
    Djarmati, Ana
    Hagenah, Johann
    Reetz, Kathrin
    Winkler, Susen
    Behrens, Maria Isabel
    Pawlack, Heike
    Lohmann, Katja
    Ramirez, Alfredo
    Tadic, Vera
    Brueggemann, Norbert
    Berg, Daniela
    Siebner, Hartwig R.
    Lang, Anthony E.
    Pramstaller, Peter P.
    Binkofski, Ferdinand
    Kostic, Vladimir S.
    Volkmann, Jens
    Gasser, Thomas
    Klein, Christine
    MOVEMENT DISORDERS, 2009, 24 (14) : 2104 - 2111
  • [4] PTPA variants are rare in early-onset and familial Parkinson's disease
    Dulski, Jaroslaw
    Soto-Beasley, Alexandra, I
    Uitti, Ryan J.
    Wszolek, Zbigniew K.
    Ross, Owen A.
    BRAIN, 2023, 146 (12) : E125 - E127
  • [5] Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease
    dos Santos, Adriana Vaz
    Pestana, Cristiane Pinheiro
    da Silva Diniz, Karen Rafaella
    Campos, Mario
    Abdalla-Carvalho, Claudia Bueno
    Zuma de Rosso, Ana Lucia
    Pereira, Joao Santos
    Nicaretta, Denise Hack
    de Carvalho, William Luciano
    dos Santos, Jussara Mendonca
    Santos-Reboucas, Cintia Barros
    Goncalves Pimentel, Marcia Mattos
    NEUROSCIENCE LETTERS, 2010, 485 (02) : 121 - 124
  • [6] ATP13A2 Variability in Taiwanese Parkinson's Disease
    Chen, Chiung-Mei
    Lin, Chih-Hsin
    Juan, Hsueh-Fen
    Hu, Fen-Ju
    Hsiao, Ya-Chin
    Chang, Hsin-Yi
    Chao, Chih-Ying
    Chen, I-Cheng
    Lee, Li-Ching
    Wang, Tsu-Wei
    Chen, Ya-Tang
    Chen, Yi-Tsun
    Lee-Chen, Guey-Jen
    Wu, Yih-Ru
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2011, 156B (06) : 720 - 729
  • [7] Lysosomal defects in ATP13A2 and GBA associated familial Parkinson’s disease
    Shigeto Sato
    Yuanzhe Li
    Nobutaka Hattori
    Journal of Neural Transmission, 2017, 124 : 1395 - 1400
  • [8] Genetic characterization of ATP13A2 in Parkinson's disease
    Vilarino-Guell, C.
    Soto, A. I.
    Hulihan, M. M.
    Ishihara-Paul, L.
    Amouri, R.
    Yahmed, S. B.
    Kefi, M.
    Middleton, L. T.
    Gibson, R. A.
    Hentati, E.
    Farrer, M. J.
    PARKINSONISM & RELATED DISORDERS, 2007, 13 : S96 - S96
  • [9] Lysosomal defects in ATP13A2 and GBA associated familial Parkinson's disease
    Sato, Shigeto
    Li, Yuanzhe
    Hattori, Nobutaka
    JOURNAL OF NEURAL TRANSMISSION, 2017, 124 (11) : 1395 - 1400
  • [10] ATP13A2 Gene Variants in Patients with Parkinson's Disease in Xinjiang
    Wang, Dan
    Gao, Hua
    Li, Yanxia
    Jiang, Sen
    Yang, Xinling
    BIOMED RESEARCH INTERNATIONAL, 2020, 2020
12345