Physiological genomics identifies genetic modifiers of long QT syndrome type 2 severity-Reference-Cited by-同舟云学术

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Physiological genomics identifies genetic modifiers of long QT syndrome type 2 severity

Published:2018-02-12 Issue:3 Volume:128 Page:1043-1056
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Chai Sam,Wan Xiaoping,Ramirez-Navarro Angelina,Tesar Paul J.,Kaufman Elizabeth S.,Ficker Eckhard,George Alfred L.,Deschênes Isabelle

Funder

NHLBI

American Heart Association

National Center for Advancing Translational Sciences

All funding sources are listed below

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://www.jci.org/articles/view/94996/files/pdf

Reference53 articles.

1. Genetic and Molecular Basis of Cardiac Arrhythmias: Impact on Clinical Management Parts I and II

2. The QT syndromes: long and short

3. Prevalence of the Congenital Long-QT Syndrome

4. Molecular and genetic basis of sudden cardiac death

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

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1. Ion occupancy of the selectivity filter controls opening of a cytoplasmic gate in the K2P channel TALK-2;Nature Communications;2024-08-30

2. From genes to clinical management: A comprehensive review of long QT syndrome pathogenesis and treatment;Heart Rhythm O2;2024-08

3. Gene and stem cell therapy for inherited cardiac arrhythmias;Pharmacology & Therapeutics;2024-04

4. Ventricular Tachycardia Due to Triggered Activity;JACC: Clinical Electrophysiology;2023-12

5. Ion occupancy of the selectivity filter controls opening of a cytoplasmic gate in the K2P channel TALK-2;2023-11-22

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