登录 注册 会员服务 联系我们

A new arginine substitution mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria

  • Published:2005-02 Issue:2 Volume:37 Page:95-99
  • ISSN:0923-1811
  • Container-title:Journal of Dermatological Science
  • language:en
  • Short-container-title:Journal of Dermatological Science

Author:

Li Cheng-Rang,Li Ming,Ma Hui-Jun,Luo Dan,Yang Li-Jia,Wang Da-Guang,Zhu Xiao-Hong,Yue Xue-Zhuang,Chen Wen-Qi,Zhu Wen-Yuan

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference16 articles.

1. Reticulate acropigmentation of Dohi;Ostlere;Clin. Exp. Dermatol.,1995

2. An unknown disorder of hyperpigmentation (in Japanese);Toyama;Jpn. J. Dermatol. Urol.,1910

3. Dyschromatosis symmetrica hereditaria (in Japanese);Toyama;Jpn. J. Dermatol. Urol.,1929

4. Seven novel mutations of the ADAR gene in chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH);Zhang;Hum. Mutat.,2004

5. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases;Oyama;Br. J. Dermatol.,1999

Cited by 22 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3