A young boy with ventricular arrhythmias and thyroid dysgenesis: two genes are not enough?
Author:
Publisher
Archives of Endocrinology and Metabolism
Subject
Endocrinology, Diabetes and Metabolism
Reference28 articles.
1. The genetics of congenital heart disease: a review of recent developments;Weismann;Curr Opin Cardiol,2007
2. Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease;Kasahara;J Clin Invest,2000
3. Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation;Yu;Int J Med Sci,2014
4. Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia;Perera;Pediatr Cardiol,2014
5. Expanding the electrical phenotype of NKX2-5 mutations: Ventricular tachycardia, atrial fibrillation, and complete heart block within one family;Jhaveri;Heart Rhythm Case Rep,2018
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