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

[Single nucleotide polymorphism in SCN5A and the distribution in Chinese Han ethnic group].

Sheng li xue bao : [Acta physiologica Sinica] - 25 Feb 2004

Xie Xu-Dong, Wang Xing-Xiang, Chen Jun-Zhu, Tao Ming, Shang Yun-Peng, Guo Xiao-Gang, Zheng Liang-Rong

Abstract excerpt

Mutations in voltage-gated sodium channel type (SCN5A) may evoke severe, life-threatening disturbances in cardiac rhythm, including long QT syndrome, idiopathic ventricular fibrillation (Brugada Syndrome), and isolated cardiac conduction disease. There is increasing awareness of the role of common polymorphisms in altering gene function and in susceptibility to diseases. The aim of the present study was to...

Read the complete abstract on PubMed

Topics

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

Share to Arrhythmias, Cardiac
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Gene Frequency

Share to Myocardium

Share to Point Mutation

Share to Polymorphism, Single Nucleotide

Share to Sodium Channels

Source

Identifiers

PMID: 14985827

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

[Single nucleotide polymorphism in SCN5A and the distribution in Chinese Han ethnic group].PMID 14985827Read ↗

Single nucleotide polymorphisms of the SCN5A gene in Han Chinese and their relation with Brugada syndrome.Semantic proximity Read ↗

Association of human SCN5A polymorphisms with idiopathic ventricular arrhythmia in a Chinese Han cohort.Semantic proximity Read ↗

[Association of single nucleotide polymorphism in human SCN7A gene with essential hypertension in Chinese].Semantic proximity Read ↗

Genetic polymorphisms and haplotypes of the human cardiac sodium channel alpha subunit gene (SCN5A) in Japanese and their association with arrhythmia.Semantic proximity Read ↗

Genetic analysis of cardiac SCN5A Gene in Iranian patients with hereditary cardiac arrhythmias.Semantic proximity Read ↗

Single nucleotide polymorphisms and haplotype of four genes encoding cardiac ion channels in Chinese and their association with arrhythmia.Semantic proximity Read ↗

[Novel SCN5A gene mutations associated with Brugada syndrome: V95I, A1649V and delF1617].Semantic proximity Read ↗

Mutations in the SCN5A gene: evidence for a link between long QT syndrome and sudden death?Semantic proximity Read ↗

A1180V of cardiac sodium channel gene (SCN5A): is it a risk factor for dilated cardiomyopathy or just a common variant in Han Chinese?Semantic proximity Read ↗

[Polymorphisms of the SCN10A Gene in Patients With Sick Sinus Syndrome].Semantic proximity Read ↗

Identification of a novel missense SCN5A mutation in a Chinese Han family with Brugada syndrome.Semantic proximity Read ↗

Whole-exome sequencing identifies a Novel SCN5A mutation (C335R) in a Chinese family with arrhythmia.Semantic proximity Read ↗

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