Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population

被引：0

作者：

Juan Zhang

Mei-Jiao Chen

Gui-Xian Zhao

Hong-Fu Li

Lei Wu

Yong-Feng Xu

Yajin Liao

Zengqiang Yuan

Zhi-Ying Wu

机构：

[1] Zhejiang University School of Medicine,Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province

[2] Fudan University,Department of Neurology and Institute of Neurology, Huashan Hospital, Shanghai Medical College

[3] Fujian Medical University,Department of Neurology, First Affiliated Hospital

[4] Beijing Institute of Basic Medical Sciences,The Brain Science Center

来源：

Journal of Neurology | 2021年 / 268卷

关键词：

Neuromyelitis optica spectrum disorder; Multiple sclerosis; Chinese;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：506 / 515

页数：9

共 50 条

[1] Common genetic variants inPRRC2Aare associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population
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