Article
Translation reinitiation in c.453delC frameshift mutation of KCNH2 producing functional hERG K+ channels with mild dominant negative effect in the heterozygote patient-derived iPSC cardiomyocytes.
Human molecular genetics - 7 Jan 2024
Park Na Kyeong, Park Soon-Jung, Park Yun-Gwi, Moon Sung-Hwan, Woo JooHan, Kim Hyun Jong, Kim Sung Joon, Choi Seong Woo
Abstract excerpt
The c.453delC (p.Thr152Profs*14) frameshift mutation in KCNH2 is associated with an elevated risk of Long QT syndrome (LQTS) and fatal arrhythmia. Nevertheless, the loss-of-function mechanism underlying this mutation remains unexplored and necessitates an understanding of electrophysiology. To gain insight into the mechanism of the LQT phenotype, we conducted whole-cell patch-clamp and immunoblot assays,...
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