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

TNNT2 gene polymorphisms are associated with susceptibility to idiopathic dilated cardiomyopathy in the Han Chinese population.

BioMed research international - 1 Jan 2013

Li Xiaoping, Wang Huan, Luo Rong, Gu Haiyong, Zhang Channa, Zhang Yu, Hui Rutai, Wu Xiushan, Hua Wei

Abstract excerpt

BACKGROUND: Idiopathic dilated cardiomyopathy (DCM) is characterized by ventricular chamber enlargement and systolic dysfunction. The pathogenesis of DCM remains uncertain, and the TNNT2 gene is potentially associated with DCM. To assess the role of TNNT2 in DCM, we examined 10 tagging single nucleotide polymorphisms (SNPs) in the patients. METHODS: A total of 97 DCM patients and 189 control subjects were...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathy, Dilated
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Genetic Predisposition to Disease

Share to Linkage Disequilibrium

Share to Polymorphism, Single Nucleotide

Share to Troponin T

Source

Open in PubMed Open full text

Identifiers

PMID: 23586019
DOI: 10.1155/2013/201372
PMCID: PMC3613050

Genes

TNNT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

TNNT2 gene polymorphisms are associated with susceptibility to idiopathic dilated cardiomyopathy in the Han Chinese population.PMID 23586019Read ↗

Cardiac troponin T (TNNT2) mutations in chinese dilated cardiomyopathy patients.Semantic proximity Read ↗

TNNT2 Gene Polymorphisms are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in Kazak and Han Chinese.Semantic proximity Read ↗

Association of genetic polymorphisms on BTNL2 with susceptibility to and prognosis of dilated cardiomyopathy in a Chinese population.Semantic proximity Read ↗

Next-Generation Sequencing Reveals Novel Genetic Variants for Dilated Cardiomyopathy in Pediatric Chinese Patients.Semantic proximity Read ↗

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.Semantic proximity Read ↗

Genetic characterization of dilated cardiomyopathy patients undergoing heart transplantation in the Chinese population by whole-exome sequencing.Semantic proximity Read ↗

Next-Generation Sequencing Screening Reveals Novel Genetic Variants for Dilated Cardiomyopathy in Pediatric Chinese PatientsSemantic proximity Read ↗

Genetic Basis and Genotype–Phenotype Correlations in Han Chinese Patients with Idiopathic Dilated CardiomyopathySemantic proximity Read ↗

Genetic analysis using targeted next-generation sequencing of sporadic Chinese patients with idiopathic dilated cardiomyopathy.Semantic proximity Read ↗

Association between MMP2 gene polymorphisms and dilated cardiomyopathy in a Chinese Han population.Semantic proximity Read ↗

Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.Semantic proximity Read ↗

Genetic variation screening of TNNT2 gene in a cohort of patients with hypertrophic and dilated cardiomyopathy.Semantic proximity Read ↗

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