您当前的位置:
首页 >
文章列表页 >
Novel Mutation of WFS1 Gene in One Pediatric Case of Wolfram Syndrome
更新时间:2023-08-23
    • Novel Mutation of WFS1 Gene in One Pediatric Case of Wolfram Syndrome

    • Vol. 29, Issue 8, Pages: 35-37(2023)
    • 作者机构:

      深圳市儿童医院,广东,深圳,518026

    • DOI:10.13407/j.cnki.jpp.1672-108X.2023.08.010    

      CLC:
    • Published:2023,

      Published Online:10 August 2023,

    扫 描 看 全 文

  • Jia Shilei, Chen Rendian, Gao Xiaojie, et al. Novel Mutation of WFS1 Gene in One Pediatric Case of Wolfram Syndrome. [J]. 29(8):35-37(2023) DOI: 10.13407/j.cnki.jpp.1672-108X.2023.08.010.

  •  
  •  
查看原文

0

Views

153

下载量

0

CSCD

Alert me when the article has been cited
提交
Tools
Download
Export Citation
Share
Add to favorites
Add to my album

Related Articles

A Case of Legius Syndrome Complicated with Epilepsy and Literature Review
A Case of Moyamoya Disease Induced by RNF213 Gene and Literature Review
Identification and Phenotypic Analysis of a Case of DES Gene Mutation Characterized by Cardiac Involvement

Related Author

Zhang Xuan
Ji Haonan
Gu Ruiyin
Li Bin
Zhou Hui
Suo Guihai
Zheng Yuqin
Wu Youjia

Related Institution

Affiliated Hospital of Nantong University
Children’s Hospital of Shanghai Jiaotong University, Children’s Hospital of Shanghai
0