Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness

Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness

<i>KCNQ1</i> encodes the voltage-gated potassium (Kv) channel KCNQ1, also known as KvLQT1 or Kv7.1. Together with its ß-subunit KCNE1, also denoted as minK, this channel generates the slowly activating cardiac delayed rectifier current <i>I</i><sub>Ks</sub>, which...

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Bibliographic Details
Main Authors: Annemarie Oertli, Susanne Rinné, Robin Moss, Stefan Kääb, Gunnar Seemann, Britt-Maria Beckmann, Niels Decher
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:International Journal of Molecular Sciences
Subjects:
KCNQ1
LQTS
potassium channel
electrophysiology
Online Access:https://www.mdpi.com/1422-0067/22/3/1112

Internet

https://www.mdpi.com/1422-0067/22/3/1112

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