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

[Correlation of cardiac troponin T gene mutations to hypertrophic cardiomyopathy in Chinese patients].

Nan fang yi ke da xue xue bao = Journal of Southern Medical University - 1 Sept 2011

Li Min, Cheng Kuan, Wang Qi-bing, Zhu Wen-qing, Chen Rui-zhen, Ge Jun-bo, Chen Hao-zhu

Abstract excerpt

OBJECTIVE: To study cardiac troponin T (TNNT2) gene mutations in Chinese patients with hypertrophic cardiomyopathy (HCM) and analyze the correlation between the genotype and phenotype. METHODS: Ninety-five unrelated Chinese patients with HCM and 120 control individuals were screened for TNNT2 gene mutations. Seven exons (8, 9, 10, 11, 14, 15, and 16) in the functional regions of TNNT2 gene were amplified using...

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 Cardiomyopathy, Hypertrophic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to TNNT2 gene

Share to Mutation

Share to Troponin T

Source

Identifiers

PMID: 21945774

Genes

TNNT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Correlation of cardiac troponin T gene mutations to hypertrophic cardiomyopathy in Chinese patients].PMID 21945774Read ↗

[Novel mutations of cardiac troponin T in Chinese patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

[Family hypertrophic cardiomyopathy caused by a 14035c > t mutation in cardiac troponin T gene].Semantic proximity Read ↗

[Association of TNNT2 gene mutations with idiopathic dilated cardiomyopathy in a Chengdu population].Semantic proximity Read ↗

[Analysis of MYH7, MYBPC3 and TNNT2 gene mutations in 10 Chinese pedigrees with familial hypertrophic cardiomyopathy and the correlation between genotype and phenotype].Semantic proximity Read ↗

Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

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

[A novel missense mutation, K124N, in the troponin T gene of Chinese populations with hypertrophic cardiomyopathy].Semantic proximity Read ↗

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

[Mutations in beta myosin heavy chain gene: two mutations in Chinese with familial hypertrophic cardiomyopathy and the correlation between the genotype and phenotype].Semantic proximity Read ↗

Cardiac Troponin T (TNNT2) mutations are less prevalent in Indian hypertrophic cardiomyopathy patients.Semantic proximity Read ↗

[Comparative study of gene mutation between Chinese patients with familial and sporadic hypertrophic cardiomyopathy].Semantic proximity Read ↗

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

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