Mutation Detection in Congenital Long QT Syndrome
Author:
Publisher
Humana Press
Link
http://link.springer.com/content/pdf/10.1007/978-1-59745-159-8_13.pdf
Reference14 articles.
1. Curran, M. E., Splawski, I., Timothy, K. W., Vincent, G. M., Green, E. D., and Keating, M. T. (1995) A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 80, 795–803.
2. Wang, Q., Shen, J., Splawski, I., et al. (1995) SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 80, 805–811.
3. Splawski, I., Shen, J., Timothy, K. W., et al. (2000) Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation 102, 1178–1185.
4. Tester, D. J., Will, M. L., Haglund, C. M., and Ackerman, M. J. (2005) Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing. Heart Rhythm 2, 507–517.
5. Keating, M. T. and Sanguinetti, M. C. (2001) Molecular and cellular mechanisms of cardiac arrhythmias. Cell 104, 569–580.
Cited by 20 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. Contemporary genetic testing in inherited cardiac disease;Journal of Cardiovascular Medicine;2018-01
2. The Promise and Peril of Precision Medicine;Mayo Clinic Proceedings;2016-11
3. Sudden Cardiac Arrest in Pediatrics;Pediatric Emergency Care;2016-09
4. Long QT syndrome, cardiovascular anomaly and findings in ECG-guided genetic testing;IJC Heart & Vessels;2014-09
5. A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation;Heart Rhythm;2014-03
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