Does knowledge of the mutation in hereditary long QT syndrome aid risk stratification?

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

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Corrections and comments

• Comment on
  Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region.2021

Authors and funding

1 author.

Funding

Abstract

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