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

Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy.

American heart journal - 1 Oct 2013

Marsiglia Julia Daher Carneiro, Credidio Flávia Laghi, de Oliveira Théo Gremen Mimary, Reis Rafael Ferreira, Antunes Murillo de Oliveira, de Araujo Aloir Queiroz, Pedrosa Rodrigo Pinto, Barbosa-Ferreira João Marcos Bemfica, Mady Charles, Krieger José Eduardo, Arteaga-Fernandez Edmundo, Pereira Alexandre da Costa

Abstract excerpt

BACKGROUND: Hypertrophic cardiomyopathy (HC) is the most prevalent genetic cardiac disease caused by a mutation in sarcomeres, Z-disks, or calcium-handling genes and is characterized by unexplained left ventricular hypertrophy. The aim of this study was to determine the genetic profile of Brazilian patients with HC and correlate the genotype with the phenotype. METHODS: We included 268 index patients from São...

Read the complete abstract on PubMed

Topics

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

Share to Brazil
Share to Cardiac Myosins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiomyopathy, Hypertrophic

Share to Carrier Proteins

Share to Myosin Heavy Chains

Share to Myosins

Share to Prevalence

Share to Troponin T

Source

Identifiers

PMID: 24093860
DOI: 10.1016/j.ahj.2013.07.029

Genes

MYBPC3
MYH7
TNNT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy.PMID 24093860Read ↗

Spectrum and clinical manifestations of mutations in genes responsible for hypertrophic cardiomyopathy.Semantic proximity Read ↗

Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional Study.Semantic proximity Read ↗

Genetic and Clinical Characterization of a South-Brazilian Hypertrophic Cardiomyopathy Cohort.Semantic proximity Read ↗

Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

Clinical predictors of a positive genetic test in hypertrophic cardiomyopathy in the Brazilian population.Semantic proximity Read ↗

A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

Sarcomeric hypertrophic cardiomyopathy: genetic profile in a Portuguese population.Semantic proximity Read ↗

[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

Molecular Diagnosis of Hypertrophic Cardiomyopathy (HCM): In the Heart of Cardiac DiseaseSemantic proximity Read ↗

Role of Genetics in Diagnosis and Management of Hypertrophic Cardiomyopathy: A Glimpse into the FutureSemantic proximity Read ↗

Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients.Semantic proximity Read ↗

Early results of sarcomeric gene screening from the Egyptian National BA-HCM Program.Semantic proximity Read ↗

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