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

Multiple genetic variants in adolescent patients with left ventricular noncompaction cardiomyopathy.

International journal of cardiology - 1 Mar 2020

Liu Shenghua, Xie Yuanyuan, Zhang Hongliang, Feng Zongqi, Huang Jian, Huang Jie, Hu Shengshou, Wei Yingjie

Abstract excerpt

BACKGROUND: Left ventricular noncompaction cardiomyopathy (LVNC) is a primary cardiomyopathy with an unclear aetiology. The clinical symptoms range from asymptomatic to heart failure, arrhythmias and sudden cardiac death. This study aimed to characterize the genetic features and clinical outcomes of LVNC who underwent heart transplantation (HTx) to reveal the potential genetic pathogenesis. METHODS AND RESULTS:...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Echocardiography

Share to Exome Sequencing

Share to Isolated Noncompaction of the Ventricular Myocardium

Share to Phenotype

Share to Young Adult

Source

Identifiers

PMID: 31918855
DOI: 10.1016/j.ijcard.2019.12.001

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

Multiple genetic variants in adolescent patients with left ventricular noncompaction cardiomyopathy.PMID 31918855Read ↗

A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction.Semantic proximity Read ↗

Molecular analysis of dilated and left ventricular noncompaction cardiomyopathies in Egyptian children.Semantic proximity Read ↗

Genetic architecture of left ventricular noncompaction in adultsSemantic proximity Read ↗

Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologiesSemantic proximity Read ↗

Genetic Profile of Left Ventricular Noncompaction Cardiomyopathy in Children—A Single Reference Center ExperienceSemantic proximity Read ↗

Increased Burden of Ion Channel Gene Variants Is Related to Distinct Phenotypes in Pediatric Patients With Left Ventricular Noncompaction.Semantic proximity Read ↗

Genetic Basis of Left Ventricular Noncompaction.Semantic proximity Read ↗

Inherited CardiomyopathiesSemantic proximity Read ↗

Genetic Basis of Childhood CardiomyopathySemantic proximity Read ↗

Left ventricular noncompaction: a distinct cardiomyopathy or a trait shared by different cardiac diseases?Semantic proximity Read ↗

Genetic Analysis of Patients with Left Ventricular Noncompaction: Identification of Novel Candidate VariantsSemantic proximity Read ↗

Genotype‐Positive Status Is Associated With Poor Prognoses in Patients With Left Ventricular Noncompaction CardiomyopathySemantic proximity Read ↗

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