Confirmation of a Causal Role for SHQ1 Variants in Early Infantile-Onset Recessive Dystonia

被引:7
|
作者
Indelicato, Elisabetta [1 ]
Boesch, Sylvia [1 ]
Baumgartner, Manuela [2 ]
Plecko, Barbara [3 ]
Winkelmann, Juliane [4 ,5 ,6 ,7 ]
Zech, Michael [4 ,5 ,8 ]
机构
[1] Med Univ Innsbruck, Dept Neurol, Innsbruck, Austria
[2] Ordensklinikum Linz Barmherzige Schwestern, Abt Entwicklungsneurol & Neuropadiatrie, Linz, Austria
[3] Med Univ Graz, Dept Paediat & Adolescent Med, Div Gen Paediat, Graz, Austria
[4] Helmholtz Zentrum Munchen, Inst Neurogenom, Munich, Germany
[5] Tech Univ Munich, Inst Human Genet, Sch Med, Munich, Germany
[6] Tech Univ Munich, Lehrstuhl Neurogenet, Munich, Germany
[7] Munich Cluster Syst Neurol SyNergy, Munich, Germany
[8] Helmholtz Zentrum Munchen Deutsch Forschungszentr, Inst Neurogenom, Ingolstadter Landstr 1, D-85764 Neuherberg, Germany
关键词
dystonia; infantile-onset movement disorder; SHQ1; translational control;
D O I
10.1002/mds.29281
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:355 / 357
页数:3
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