Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias-Reference-Cited by-同舟云学术

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Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias

Published:1997-10-01 Issue:11 Volume:6 Page:1943-1949
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Wollnik B.,Schroeder B. C.,Kubisch C.,Esperer H. D.,Wieacker P.,Jentsch T. J.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/6/11/1943/2008183/6-11-1943.pdf

Reference28 articles.

1. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death

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

3. KVLQT1 mutations in three families with familial or sporadic long QT syndrome

4. Four Novel KVLQT1 and Four Novel HERG Mutations in Familial Long-QT Syndrome

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1. Identification and in-silico characterization of splice-site variants from a large cardiogenetic national registry;European Journal of Human Genetics;2022-09-22

2. EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- and Kir5.1-Associated Channelopathies;Frontiers in Physiology;2022-03-15

3. A novel KCNQ4 gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non‑syndromic deafness 2A;Molecular Medicine Reports;2021-04-01

4. Age-related hearing loss pertaining to potassium ion channels in the cochlea and auditory pathway;Pflügers Archiv - European Journal of Physiology;2020-12-17

5. Genetic homozygosity in a diverse population: An experience of long QT syndrome;International Journal of Cardiology;2020-10

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