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Article

Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome.

International journal of cardiology - 1 Jan 2015

Harrell Daniel Toshio, Ashihara Takashi, Ishikawa Taisuke, Tominaga Ichiko, Mazzanti Andrea, Takahashi Kazuhiro, Oginosawa Yasushi, Abe Haruhiko, Maemura Koji, Sumitomo Naokata, Uno Kikuya, Takano Makoto, Priori Silvia G, Makita Naomasa

Abstract excerpt

BACKGROUND: Short QT syndrome (SQTS) is a rare inheritable arrhythmia, associated with atrial and ventricular fibrillations, caused by mutations in six cardiac ion channel genes with high penetrance. However, genotype-specific clinical differences between SQTS patients remain to be elucidated. ME...

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Source

Identifiers

PMID: 25974115
DOI: 10.1016/j.ijcard.2015.04.090

Genes

KCNH2
KCNQ1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25974115-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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