July 2, 2022Open Access

Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes

Key Result

Mutation-specific variants in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) channels drive distinct Long QT Syndrome phenotypes, supporting a layered precision medicine approach.

Main Result

Absolute Event Rate: 0% vs 0%

Abstract

variants, with the goal of realizing a layered precision medicine approach focused on individuals.

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Cite This Study

Kekenes–Huskey et al. (Sat,) reported a other. Mutation-specific variants in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) channels drive distinct Long QT Syndrome phenotypes, supporting a layered precision medicine approach.

synapsesocial.com/papers/6a07e2c1416812afca06e6b6 https://doi.org/https://doi.org/10.3390/ijms23137389

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