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

[Identification of an SCN5A mutation in a Chinese pedigree with a history of syncope].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 4 May 2017

Wang J, Dai G Y, Qin Y M

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Mutation
Share to NAV1.5 Voltage-Gated Sodium Channel
Share to Pedigree

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Syncope

Source

Identifiers

PMID: 28482396
DOI: 10.3760/cma.j.issn.0578-1310.2017.05.019

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Identification of an SCN5A mutation in a Chinese pedigree with a history of syncope].PMID 28482396Read ↗

[Familial cardiomyopathy caused by mutation of SCN5A gene].Semantic proximity Read ↗

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

[The cardiac sodium channel gene SCN5A mutation and dilated cardiomyopathy].Semantic proximity Read ↗

Whole‑exome sequencing identifies a novel mutation (R367G) in SCN5A to be associated with familial cardiac conduction disease.Semantic proximity Read ↗

[Screening of genetic mutations in a Chinese pedigree affected with hypokalemic periodic paralysis].Semantic proximity Read ↗

Familial Dilated Cardiomyopathy and Sudden Cardiac Arrest: New Association with a SCN5A Mutation.Semantic proximity Read ↗

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeSemantic proximity Read ↗

SCN5A R1193Q polymorphism associated with progressive cardiac conduction defects and long QT syndrome in a Chinese family.Semantic proximity Read ↗

[A novel mutation of SCN4A gene causes hypokalemic periodic paralysis in a Chinese family].Semantic proximity Read ↗

[A case of long QT syndrome with atypical clinical phenotype caused by KCNQ1-R555C missense mutation].Semantic proximity Read ↗

[A Chinese pedigree with hypertrophic cardiomyopathy caused by rare homozygous mutation of TNNI3 gene p.Arg162Gln].Semantic proximity Read ↗

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

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