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
收藏
页码：506 / 515
页数：9
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