The Discovery of LRRK2 Mutations as a Cause of Parkinson's Disease

被引：4
作者：
Singleton, Andrew B. [1 ]
Gasser, Thomas [2 ,3 ,4 ]
机构：
[1] NIA, Neurogenet Lab, Bethesda, MD 20892 USA
[2] Univ Tubingen, Dept Neurodegenerat, Ctr Neurol, Tubingen, Germany
[3] Univ Tubingen, Hertie Inst Clin Brain Res, Tubingen, Germany
[4] Univ Tubingen, German Ctr Neurodegenerat Dis, Tubingen, Germany
来源：
MOVEMENT DISORDERS | 2020年 / 35卷 / 04期
基金：
美国国家卫生研究院;
关键词：
GENE; FAMILIES; LOCUS;
D O I：
10.1002/mds.27999
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：551 / 554
页数：4
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