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

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

Objectives: This study assessed the phenotypic variability of LQTS in carriers with the same and with different mutations in the LQT2 gene. Background: Mutations of ion‐channel genes are known to cause the long QT syndrome (LQTS), a disorder associated with distinctive genotypic‐specific electrocard...

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Bibliographic Details
Main Authors: Jesaia Benhorin, Arthur J. Moss, Matthew Bak, Wojciech Zareba, Elizabeth S. Kaufman, Batsheva Kerem, Jeffrey A. Towbin, Silvia Priori, Robert S. Kass, Bernard Attali, Arthur M. Brown, Eckhard Ficker
Format: Article
Language:English
Published: Wiley 2001-01-01
Series:Annals of Noninvasive Electrocardiology
Subjects:
long QT syndrome
genes
electrocardiography
HERG
Online Access:https://doi.org/10.1111/j.1542-474X.2001.tb00137.x

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https://doi.org/10.1111/j.1542-474X.2001.tb00137.x

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