Variable Expression of Long QT Syndrome Among Gene Carriers from Families with Five Different HERG Mutations-Reference-Cited by-同舟云学术

Variable Expression of Long QT Syndrome Among Gene Carriers from Families with Five Different HERG Mutations

Published:2001-01 Issue:1 Volume:7 Page:40-46
ISSN:1082-720X
Container-title:Annals of Noninvasive Electrocardiology
language:en
Short-container-title:Annals of Noninvasive Electrocardiology

Author:

Benhorin Jesaia¹,Moss Arthur J.²,Bak Matthew²,Zareba Wojciech²,Kaufman Elizabeth S.³,Kerem Batsheva⁴,Towbin Jeffrey A.⁵,Priori Silvia⁶,Kass Robert S.⁷,Attali Bernard⁸,Brown Arthur M.³,Ficker Eckhard³

Affiliation:

1. Department of Cardiology, Bikur Cholim Hospital, Israel

2. Cardiology Unit, Department of Medicine, University of Rochester Medical Center, Rochester, New York

3. The Heart and Vascular Research Center, MetroHealth Campus, Case Western Reserve University, Cleveland, Ohio

4. Department of Genetics, The Life Sciences Institute, The Hebrew University, Jerusalem, Israel

5. Department of Pediatric Cardiology, Baylor College of Medicine, Houston, Texas

6. Molecular Cardiology, Fondazione S. Maugeri‐University of Pavia, Pavia, Italy

7. Department of Pharmacology, College of Physicians and Surgeons, Columbia University, New York, New York

8. Departments of Physiology and Pharmacology, Sackler Medical School, Tel‐Aviv, Israel

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1542-474X.2001.tb00137.x

Reference22 articles.

1. WardOC.New familial cardiac syndrome in children.J Ir Med Assoc1964;103–106.

2. The long Q-T syndrome

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

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

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

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