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

Analysis of MEF2A mutations in a Chinese population with premature coronary artery disease.

Genetic testing and molecular biomarkers - 1 Apr 2013

Dai Yuxiang, Zhang Shuyang, Wu Wei

Abstract excerpt

AIMS: To assess the relationship between mutations of the myocyte enhancer factor 2A (MEF2A) and premature coronary artery disease (PCAD) in a Chinese population. METHODS AND RESULTS: The mutations in the exons 8 and 12 of the MEF2A gene were analyzed in both PCAD families and sporadic cases using direct sequencing of polymerase chain reaction products. In one PCAD family, seven members of the third generation...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Asian People
Share to Coronary Artery Disease

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to MADS Domain Proteins

Share to MEF2 Transcription Factors

Share to Myogenic Regulatory Factors

Share to Pedigree

Source

Identifiers

PMID: 23461724
DOI: 10.1089/gtmb.2012.0467

Genes

CAD

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

Analysis of MEF2A mutations in a Chinese population with premature coronary artery disease.PMID 23461724Read ↗

Novel 6-bp deletion in MEF2A linked to premature coronary artery disease in a large Chinese family.Semantic proximity Read ↗

MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population.Semantic proximity Read ↗

Variants in exon 11 of MEF2A gene and coronary artery disease: evidence from a case-control study, systematic review, and meta-analysis.Semantic proximity Read ↗

MEF2A gene and susceptibility to coronary artery disease in the Chinese people.Semantic proximity Read ↗

Exon 11 deletion in the myocyte enhancer factor (MEF)2A and early onset coronary artery disease gene in a Sicilian family.Semantic proximity Read ↗

A study of the role of the Myocyte-specific Enhancer Factor-2A gene in coronary artery disease.Semantic proximity Read ↗

Relationship of the CAG repeat polymorphism of the MEF2A gene and coronary artery disease in a Chinese population.Semantic proximity Read ↗

Lack of MEF2A mutations in coronary artery disease.Semantic proximity Read ↗

[Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease].Semantic proximity Read ↗

Assessment of MEF2A mutations in myocardial infarction in Japanese patients.Semantic proximity Read ↗

Structural changes in exon 11 of MEF2A are not related to sporadic coronary artery disease in Han Chinese population.Semantic proximity Read ↗

MEF2A sequence variants and coronary artery disease: a change of heart?Semantic proximity Read ↗

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