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

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

Heart and vessels - 1 Nov 2013

Fujita Etsuko, Nakanishi Toshio, Nishizawa Tsutomu, Hagiwara Nobuhisa, Matsuoka Rumiko

Abstract excerpt

Hypertrophic cardiomyopathy (HCM) is an autosomal dominant disorder resulting from mutations in genes for at least 15 various sarcomere-related proteins including cardiac β-myosin heavy chain, cardiac myosin-binding protein C, and cardiac troponin T. The troponin T gene (TNNT2) mutation has the third incidence of familial HCM, and the genotype-phenotype correlation of this gene still remains insufficient in...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Asian People
Share to Cardiomyopathy, Hypertrophic, Familial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Death, Sudden, Cardiac

Share to Infant, Newborn

Share to Prognosis

Share to Troponin T

Source

Open in PubMed Open full text

Identifiers

PMID: 23494605
DOI: 10.1007/s00380-013-0332-3
PMCID: PMC3830204

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

Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy.PMID 23494605Read ↗

Prevalence and Distribution of Sarcomeric Gene Mutations in Japanese Patients With Familial Hypertrophic CardiomyopathySemantic proximity Read ↗

Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

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

Genetic background of Japanese patients with pediatric hypertrophic and restrictive cardiomyopathy.Semantic proximity Read ↗

Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy.Semantic proximity Read ↗

Low prevalence and variable clinical presentation of troponin I and troponin T gene mutations in hypertrophic cardiomyopathy.Semantic proximity Read ↗

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

Mutations profile in Chinese patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

A novel nonsense mutation in TNNT2 in a Chinese pedigree with hypertrophic cardiomyopathy: A case report.Semantic proximity Read ↗

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

Genetic screening and double mutation in Japanese patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

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