Tor1a Gene in GABApre Interneurons: The New Player in the "Impaired Inhibition" Game of Dystonia?

被引：2
|
作者：
Monje, Mariana H. G. [1 ,2 ]
Sanchez-Ferro, Alvaro [1 ]
机构：
[1] Hosp Univ HM Puerta Sur, HM CINAC, Madrid, Spain
[2] Univ Autonoma Madrid, Sch Med, Anat Histol & Neurosci Dept, Madrid, Spain
来源：
MOVEMENT DISORDERS | 2018年 / 33卷 / 09期
关键词：
D O I：
10.1002/mds.114
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：1408 / 1408
页数：1
相关论文
共 50 条
  • [31] Intrafamilial phenotypic variability of the DYT1 dystonia:: From asymptomatic TOR1A gene carrier status to dystonic storm
    Opal, P
    Tintner, R
    Jankovic, J
    Leung, J
    Breakefield, XO
    Friedman, J
    Ozelius, L
    MOVEMENT DISORDERS, 2002, 17 (02) : 339 - 345
  • [32] Genetic analysis of TOR1A & THAP1 genes in Indian primary dystonia patients
    Giri, Subhajit
    Naiya, Tufan
    Das, Shyamal
    Sankhla, Charulata
    Ray, Kunal
    Ray, Jharna
    MOVEMENT DISORDERS, 2014, 29 : S70 - S71
  • [33] Intrafamilial phenotypic variability of the DYT1 dystonia: From asymptomatic TOR1A gene carrier status to dystonic storm
    Opal, P
    Tintner, R
    Jankovic, J
    Leung, J
    Breakefield, A
    Friedman, J
    Ozelius, L
    ANNALS OF NEUROLOGY, 2001, 50 (03) : S21 - S21
  • [34] Association of rs1182 polymorphism in TOR1A with primary dystonia in Chinese population
    Song, W.
    Huang, R.
    Chen, K.
    Chen, Y. P.
    Cao, B.
    Yang, Y.
    Shang, H.
    MOVEMENT DISORDERS, 2012, 27 : S364 - S365
  • [35] Impaired differentiation of human induced neural stem cells by TOR1A overexpression
    Felix Stengel
    Franca Vulinovic
    Britta Meier
    Karen Grütz
    Christine Klein
    Philipp Capetian
    Molecular Biology Reports, 2020, 47 : 3993 - 4001
  • [36] New Twist Defines a Spectrum of TOR1A Neurological Disease
    Cascalho, Ana
    Goodchild, Rose E.
    MOVEMENT DISORDERS, 2018, 33 (01) : 73 - 73
  • [37] The GAG deletion in Tor1A (DYT1) is a rare cause of complex musician's dystonia
    Schmidt, Alexander
    Altenmueller, Eckart
    Jabusch, Hans-Christian
    Lee, Andre
    Wiegers, Karin
    Klein, Christine
    Lohmann, Katja
    PARKINSONISM & RELATED DISORDERS, 2012, 18 (05) : 690 - 691
  • [38] Comprehensive screening of TOR1A (DYT1) gene in early-onset dystonia patients: no evidence of allelic heterogeneity.
    Cavalier, L
    Carles, S
    Guittard, C
    Roubertie, A
    Echenne, B
    Coubes, P
    Claustres, M
    Tuffery-Giraud, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 372 - 372
  • [39] TOR1A, THAP1, and GNAL Mutational Screening in Austrian Patients With Primary Isolated Dystonia
    Zech, Michael
    Boesch, Sylvia
    Sycha, Thomas
    Mueller, Joerg
    Poewe, Werner
    Winkelmann, Juliane
    MOVEMENT DISORDERS, 2015, 30 (13) : 1853 - 1854
  • [40] Multiple founder effects in Japanese families with primary torsion dystonia harboring the GAG deletion in the TOR1A (DYT1) gene
    Ikeuchi, T
    Nomura, Y
    Segawa, M
    Ozelius, LJ
    Shimohata, T
    Tsuji, S
    NEUROGENETICS, 2002, 4 (02) : 105 - 106
12345