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Published in 2022 at "Frontiers in Pharmacology"
DOI: 10.3389/fphar.2022.1010119
Abstract: Loss of function (LOF) mutations of voltage sensitive K+ channel proteins hERG (Kv11.1) and KCNQ1 (Kv7.1) account for the majority of instances of congenital Long QT Syndrome (cLQTS) with the dominant molecular phenotype being a…
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Keywords:
analysis guides;
coupling analysis;
analysis;
evolutionary coupling ... See more keywords