A novel frameshift mutation in the <em>FERMT1</em> gene in a Chinese patient with Kindler syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A novel frameshift mutation in the FERMT1 gene in a Chinese patient with Kindler syndrome

Published:2020-09-17 Issue:5 Volume:20 Page:1-1
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Meng Li¹,Yang Xiaoqin²,Wu Yuhao²,Zhao Zijun²,Yang Lianjuan ¹,Li Ming³,Wang Xiuli²,Zhang Guolong²

Affiliation:

1. Department of Dermatological Mycology, Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, P.R. China

2. Institute of Photomedicine, Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, P.R. China

3. Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200092, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Cited by 4 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

1. Identification of a novel FERMT1 variant causing kindler syndrome and a review of the clinical and molecular genetic features in Chinese patients;Frontiers in Pediatrics;2024-09-06

2. Genetic Implications and Management of Epidermolysis Bullosa in the Saudi Arabian Population;Cureus;2024-08-12

3. Medium-chain inulin alleviates the obesity and improves systemic health in diet-induced obese mice via mediating the gut microbiome and metabolome;2023-10-17

4. Novel Discoveries in Immune Dysregulation in Inborn Errors of Immunity;Frontiers in Immunology;2021-08-27

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