Variable Clinical Appearance of the Kir2.1 Rare Variants in Russian Patients with Long QT Syndrome
Background: The <i>KCNJ2</i> gene encodes inward rectifier Kir2.1 channels, maintaining resting potential and cell excitability. Presumably, clinical phenotypes of mutation carriers correlate with ion permeability defects. Loss-of-function mutations lead to QTc prolongation with variable...
Main Authors: | Elena Zaklyazminskaya, Margarita Polyak, Anna Shestak, Mariam Sadekova, Vera Komoliatova, Irina Kiseleva, Leonid Makarov, Dmitriy Podolyak, Grigory Glukhov, Han Zhang, Denis Abramochkin, Olga S. Sokolova |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-03-01
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Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/13/4/559 |
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