Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family-Reference-Cited by-同舟云学术

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Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family

Published:1998 Issue:S1 Volume:11 Page:S184-S186
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Akimoto Kaoru,Furutani Michiko,Imamura Shin-Ichiro,Furutani Yoshiyuki,Kasanuki Hiroshi,Takao Atsuyoshi,Momma Kazuo,Matsuoka Rumiko

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference13 articles.

1. Missense mutation of the β-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy;Arai;Am J Med Genet,1995

2. Missense mutation in the pore region of HERG causes familial long QT syndrome;Benson;Circulation,1996

3. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome;Curran;Cell,1995

4. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene;Keating;Science,1991

5. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome;Moss;Circulation,1995

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1. Rescue of expression and function of long QT syndrome-causing mutant hERG channels by enhancing channel stability in the plasma membrane;Journal of Biological Chemistry;2024-08

2. Ethnic and racial differences in Asian populations with ion channelopathies associated with sudden cardiac death;Frontiers in Cardiovascular Medicine;2023-08-04

3. Differential Effects of Remdesivir and Lumacaftor on Homomeric and Heteromeric hERG Channels;Molecular Pharmacology;2023-07-07

4. Successful Management of a Young Athlete with Type 2 Long QT Syndrome by Genotype-specific Risk Stratification and Bridging Therapy with a Wearable Cardioverter Defibrillator;Internal Medicine;2022-04-15

5. Molecular pathogenesis of long QT syndrome type 2;Journal of Arrhythmia;2016-10

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