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Article

Novel KCNQ1 splicing mutation in patients with forme fruste LQT1 aggravated by hypokalemia.

Journal of cardiology - 1 Aug 2014

Imai Michiko, Nakajima Tadashi, Kaneko Yoshiaki, Niwamae Nogiku, Irie Tadanobu, Ota Masaki, Iijima Takafumi, Tange Shoichi, Kurabayashi Masahiko

Abstract excerpt

BACKGROUND: Several KCNQ1 splicing mutations have been identified in patients with type-1 long QT syndrome (LQT1). It was suggested that the clinical severity may differ according to the aberrant splicing products. There may be precipitating factors that cause cardiac events in those with a mild...

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Source

Identifiers

PMID: 24373870
DOI: 10.1016/j.jjcc.2013.11.014

Genes

KCNQ1
KCNH2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24373870-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

Related research

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Novel KCNQ1 splicing mutation in patients with forme fruste LQT1 aggravated by hypokalemia.PMID 24373870Read ↗

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