Varaico: Literature-Extracted Genetic Variants

Gene:LDB3
Variant:p.T351A
Back to variants list

LDB3

NM_007078.3:p.T351A

Associated Papers

Computational analysis of congenital heart disease associated SNPs: unveiling their impact on the gene regulatory system.

Vashisht S et al.

Bmc Genomics, 2025

39838281 (PubMed )
Supplement: 12864_2025_11232_MOESM4_ESM.xlsx › ClinVar_CHD-SNPs_uniq

Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification.

van der Meulen MH et al.

Circulation. Genomic and Precision Medicine, 2022

36178741 (PubMed )
Supplement: hcg-15-e002981-s001.pdf

Myocarditis-like Episodes in Patients with Arrhythmogenic Cardiomyopathy: A Systematic Review on the So-Called Hot-Phase of the Disease.

Bariani R et al.

Biomolecules, 2022

Inflammation and Immune Response in Arrhythmogenic Cardiomyopathy: State-of-the-Art Review.

Asatryan B et al.

Circulation, 2021

International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework.

James CA et al.

Circulation. Genomic and Precision Medicine, 2021

33831308 (PubMed )
Supplement: hcg-14-e003273-s001.pdf

Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels.

Shestak AG et al.

Frontiers in Genetics, 2021

Electrocardiographic Screening of Arrhythmogenic Cardiomyopathy in Genotype-Positive and Phenotype-Negative Relatives.

Lopez-Ayala JM et al.

Frontiers in Cardiovascular Medicine, 2021

Genetic Animal Models for Arrhythmogenic Cardiomyopathy.

Gerull B et al.

Frontiers in Physiology, 2020

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy.

Towbin JA et al.

Heart Rhythm, 2019

Toward an effective exome-based genetic testing strategy in pediatric dilated cardiomyopathy.

Herkert JC et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018

Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar.

Harrison SM et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017

28301460 (PubMed )
Supplement: NIHMS853375-supplement-Supplemental_Table_4__Consensus_classifications_for_all_211_resolved_variants.xlsx › Supplemental_Table_4

Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy.

Nouhravesh N et al.

Molecular Genetics & Genomic Medicine, 2016

Pathogenesis of Arrhythmogenic Cardiomyopathy.

Asimaki A et al.

The Canadian Journal of Cardiology, 2015

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy.

Lopez-Ayala JM et al.

Clinical Genetics, 2015

Genetics of myocarditis in arrhythmogenic right ventricular dysplasia.

Lopez-Ayala JM et al.

Heart Rhythm, 2015

Gene symbol: MLH1.

Kadiyska TK et al.

Human Genetics, 2007

Gene symbol: MUTYH.

Aretz S

Human Genetics, 2007

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."