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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Hlavní autoři:	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
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wiley 2001-01-01
Edice:	Annals of Noninvasive Electrocardiology
Témata:	long QT syndrome genes electrocardiography HERG
On-line přístup:	https://doi.org/10.1111/j.1542-474X.2001.tb00137.x
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