Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.

Chinese medical journal - 1 Jan 2014

Jimmy Juang Jyh-Ming, Chen Ching-Yu, Yeh Huei-Ming, Chiu Wei-Yih, Yu Chih-Chieh, Liu Yen-Bin, Tsai Chia-Ti, Lo Li-Wei, Yeh Shih-Fan Sherri, Lai Ling-Ping

Abstract excerpt

BACKGROUND: Congenital long QT syndrome (LQTS) is an ion channelopathy associated with genetic mutations. It is well known that most LQTS patients (91%) have a single mutation. The purpose of this study was to investigate the clinical characteristics of congenital LQTS patients with bigenic mutations in Taiwan, China. METHODS: Congenital LQTS patients were recruited consecutively at Taiwan University Hospital in...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to ERG1 Potassium Channel

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ether-A-Go-Go Potassium Channels

Share to KCNQ1 Potassium Channel

Share to Long QT Syndrome

Share to NAV1.5 Voltage-Gated Sodium Channel

Share to Potassium Channels, Voltage-Gated

Share to Young Adult

Source

Identifiers

PMID: 24762593

Genes

KCNH2
KCNQ1

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.PMID 24762593Read ↗

Congenital long QT syndromes: clinical features, molecular genetics and genetic testing.Semantic proximity Read ↗

Clinical Impact of Genetic Testing for Long QT Syndrome - Evidence From a Nationwide LQTS Registry in Japan.Semantic proximity Read ↗

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.Semantic proximity Read ↗

Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1.Semantic proximity Read ↗

Congenital long QT syndrome.Semantic proximity Read ↗

Genetic and clinical advances in congenital long QT syndrome.Semantic proximity Read ↗

Genetic homozygosity in a diverse population: An experience of long QT syndrome.Semantic proximity Read ↗

Spectrum of genetic variants detected in children tested for long QT syndrome.Semantic proximity Read ↗

Long QT syndrome: a Korean single center study.Semantic proximity Read ↗

First report of genetic variants detected in Argentinian patients with clinical Long QT Syndrome diagnosisSemantic proximity Read ↗

An NGS-based genotyping in LQTS; minor genes are no longer minor.Semantic proximity Read ↗

Common Genotypes of Long QT Syndrome in China and the Role of ECG Prediction.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.