Investigation of the Effects of the Short QT Syndrome D172N Kir2.1 Mutation on Ventricular Action Potential Profile Using Dynamic Clamp

The congenital short QT syndrome (SQTS) is a cardiac condition that leads to abbreviated ventricular repolarization and an increased susceptibility to arrhythmia and sudden death. The SQT3 form of the syndrome is due to mutations to the KCNJ2 gene that encodes Kir2.1, a critical component of channel...

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Detalles Bibliográficos
Autores principales: Du, Chunyun, Rasmusson, Randall L., Bett, Glenna C., Franks, Brandon, Zhang, Henggui, Hancox, Jules C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8806151/
https://www.ncbi.nlm.nih.gov/pubmed/35115940
http://dx.doi.org/10.3389/fphar.2021.794620

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8806151/
https://www.ncbi.nlm.nih.gov/pubmed/35115940
http://dx.doi.org/10.3389/fphar.2021.794620

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