Rare variant analysis of <em>PLXNA1</em> in Parkinson's disease in the Chinese population

您当前的位置：

首页 >

文章列表页 >

Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population

Short communication | 更新时间：2023-08-29

- Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population
- Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population
- Genes & Diseases 2023年10卷第4期
- 作者机构：
  
  Department of Neurology, Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University,Sichuan,Chengdu,China,610041
- 作者简介：
- 基金信息：
- DOI：10.1016/j.gendis.2022.08.001
  中图分类号：
- 纸质出版日期：2023，
  
  网络出版日期：2023-7-1，
扫描看全文
Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population[J]. Genes & Diseases, 2023,10(4).

Chunyu Li, Ruwei Ou, Yanbing Hou, et al. Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population[J]. Genes & Diseases, 2023,10(4).
Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population[J]. Genes & Diseases, 2023,10(4). DOI： 10.1016/j.gendis.2022.08.001.

Chunyu Li, Ruwei Ou, Yanbing Hou, et al. Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population[J]. Genes & Diseases, 2023,10(4). DOI： 10.1016/j.gendis.2022.08.001.

摘要

Abstract

关键词

Keywords

references

0

浏览量

0

下载量

0

CSCD

文章被引用时，请邮件提醒。

提交

工具集

关联资源

相关文章

暂无数据

相关作者

暂无数据

相关机构

暂无数据

⁰