Clinical, Genetic, and Electrophysiologic Characteristics of a New Pas-Domain HERG Mutation (M124R) Causing Long QT Syndrome-Reference-Cited by-同舟云学术

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Clinical, Genetic, and Electrophysiologic Characteristics of a New Pas-Domain HERG Mutation (M124R) Causing Long QT Syndrome

Published:2005-07 Issue:3 Volume:10 Page:334-341
ISSN:1542-474X
Container-title:Annals of Noninvasive Electrocardiology
language:en
Short-container-title:Annals of Noninvasive Electrocardiology

Author:

Shushi Liat,Kerem Batsheva,Goldmit Maya,Peretz Asher,Attali Bernard,Medina Aron,Towbin Jeffrey A.,Kurokawa Junko,Kass Robert S.,Benhorin Jesaia

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1542-474X.2005.00643.x/fullpdf

Reference33 articles.

1. The long Q-T syndrome

2. The long QT syndrome. Prospective longitudinal study of 328 families.

3. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

4. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

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1. An intracellular hydrophobic nexus critical for hERG1 channel slow deactivation;Biophysical Journal;2024-07

2. An intracellular hydrophobic nexus is critical for slow deactivation in hERG channels;2023-03-05

3. Molecular Pathophysiology of Congenital Long QT Syndrome;Physiological Reviews;2017-01

4. Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome;Nature Communications;2014-11-24

5. Structure of the C-terminal region of an ERG channel and functional implications;Proceedings of the National Academy of Sciences;2013-06-25

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