Functional phenotype variations of two novel K V 7.1 mutations identified in patients with Long QT syndrome-Reference-Cited by-同舟云学术

Functional phenotype variations of two novel K V 7.1 mutations identified in patients with Long QT syndrome

Published:2020-01-11 Issue:2 Volume:43 Page:210-216
ISSN:0147-8389
Container-title:Pacing and Clinical Electrophysiology
language:en
Short-container-title:Pacing Clin Electrophysiol

Author:

Hammami Bomholtz Sofia¹²,Refaat Marwan³⁴^ORCID,Buur Steffensen Annette¹²,David Jens‐Peter¹²,Espinosa Karin¹²,Nussbaum Robert⁵,Wojciak Julianne⁵,Hjorth Bentzen Bo¹²,Scheinman Melvin⁵,Schmitt Nicole¹²^ORCID

Affiliation:

1. Danish National Research Foundation Centre for Cardiac ArrhythmiaUniversity of Copenhagen Copenhagen Denmark

2. Department of Biomedical SciencesUniversity of Copenhagen Copenhagen Denmark

3. Department of Internal Medicine, Division of CardiologyAmerican University of Beirut Medical Center Beirut Lebanon

4. Department of Biochemistry and Molecular GeneticsAmerican University of Beirut Beirut Lebanon

5. Department of MedicineUniversity of California, San Francisco San Francisco California

Funder

Danmarks Grundforskningsfond

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pace.13870

Reference40 articles.

1. QTc Behavior During Exercise and Genetic Testing for the Long-QT Syndrome

2. Molecular Pathophysiology of Congenital Long QT Syndrome

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

4. Cardiac Potassium Channel Subtypes: New Roles in Repolarization and Arrhythmia

5. KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current

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