Functional study of a KCNH2 mutant: Novel insights on the pathogenesis of the LQT2 syndrome.
arrhythmia
cardiac pathophysiology
channelopathy
electrophysiology
long QT syndrome
Journal
Journal of cellular and molecular medicine
ISSN: 1582-4934
Titre abrégé: J Cell Mol Med
Pays: England
ID NLM: 101083777
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
06
02
2019
revised:
02
06
2019
accepted:
08
06
2019
pubmed:
31
7
2019
medline:
21
8
2020
entrez:
31
7
2019
Statut:
ppublish
Résumé
The K
Identifiants
pubmed: 31361068
doi: 10.1111/jcmm.14521
pmc: PMC6714209
doi:
Substances chimiques
ERG1 Potassium Channel
0
KCNH2 protein, human
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
6331-6342Informations de copyright
© 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.
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