Functional study of a KCNH2 mutant: Novel insights on the pathogenesis of the LQT2 syndrome

The K(+) voltage‐gated channel subfamily H member 2 (KCNH2) transports the rapid component of the cardiac delayed rectifying K(+) current. The aim of this study was to characterize the biophysical properties of a C‐terminus‐truncated KCNH2 channel, G1006fs/49 causing long QT syndrome type II in hete...

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Bibliografiske detaljer
Udgivet i:J Cell Mol Med
Main Authors: De Zio, Roberta, Gerbino, Andrea, Forleo, Cinzia, Pepe, Martino, Milano, Serena, Favale, Stefano, Procino, Giuseppe, Svelto, Maria, Carmosino, Monica
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2019
Fag:
Original Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6714209/
https://ncbi.nlm.nih.gov/pubmed/31361068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.14521
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