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A case of long QT syndrome with triple gene abnormalities: digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1.

Heart rhythm - 1 Apr 2013

Yoshikane Yukako, Yoshinaga Masao, Hamamoto Kunihiro, Hirose Shinichi

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Share to Electrocardiography
Share to ERG1 Potassium Channel
Share to Ether-A-Go-Go Potassium Channels
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to NAV1.5 Voltage-Gated Sodium Channel

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Source

Identifiers

PMID: 23237912
DOI: 10.1016/j.hrthm.2012.12.008

Genes

KCNH2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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A case of long QT syndrome with triple gene abnormalities: digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1.PMID 23237912Read ↗

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KCNH2 variants in a family with epilepsy and long QT syndrome: A case report and literature review.Semantic proximity Read ↗

Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote.Semantic proximity Read ↗

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[Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block].Semantic proximity Read ↗

De novo R853Q mutation of SCN2A gene and West syndrome.Semantic proximity Read ↗

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