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- W2319033734 abstract "The single-pass transmembrane protein KCNE2 or MIRP1 was once thought to be the missing accessory protein that combined with hERG to fully recapitulate the cardiac repolarising current I Kr . As a result of this role, it was an easy next step to associate mutations in KCNE2 to long QT syndrome, in which there is delayed repolarisation of the heart. Since that time however, KCNE2 has been shown to modify the behaviour of several other channels and currents, and its role in the heart and in the aetiology of long QT syndrome has become less clear. In this article, we review the known interactions of the KCNE2 protein and the resulting functional effects, and the effects of mutations in KCNE2 and their clinical role." @default.
- W2319033734 created "2016-06-24" @default.
- W2319033734 creator A5052929750 @default.
- W2319033734 creator A5083962653 @default.
- W2319033734 date "2011-12-01" @default.
- W2319033734 modified "2023-10-17" @default.
- W2319033734 title "The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome" @default.
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