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Article

Mutation in KCNE1 associated to early repolarization syndrome by modulation of slowly activating delayed rectifier K+ current.

Experimental cell research - 15 Feb 2018

Yao Hao, Ji Cheng-Cheng, Cheng Yun-Jiu, Chen Xu-Miao, Liu Li-Juan, Fan Jun, Wu Su-Hua

Abstract excerpt

BACKGROUND: Recent studies have revealed that mutation in KCNE1, β-subunits of cardiac potassium channel, involved in ventricular fibrillation. Whereas its role in early repolarization syndrome (ERS) is less well understood. OBJECTIVE: To study whether mutant in KCNE1 is associated with ERS and explore the possible underlying molecular mechanisms. METHODS: Whole genome from four unrelated families with ERS was...

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Source

Identifiers

PMID: 29395134
DOI: 10.1016/j.yexcr.2018.01.030

Genes

KCNQ1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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