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

Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.

The American journal of cardiology - 1 Jul 2004

Hermida-Prieto Manuel, Monserrat Lorenzo, Castro-Beiras Alfonso, Laredo Rafael, Soler Rafaela, Peteiro Jesus, Rodríguez Esther, Bouzas Beatriz, Alvarez Nemesio, Muñiz Javier, Crespo-Leiro Marisa

Abstract excerpt

LMNA mutations have been associated with familial or sporadic dilated cardiomyopathy (DC), with or without conduction system disease. We studied the LMNA gene in 67 consecutive patients with DC (18 had familial DC, 17 had possible familial DC, and 32 sporadic DC). From genomic DNA, coding regions...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathy, Dilated
Share to DNA Primers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Echocardiography

Share to Electrocardiography

Share to Lamin Type A

Share to Magnetic Resonance Imaging

Share to Pedigree

Share to Ventricular Dysfunction, Left

Source

Identifiers

PMID: 15219508
DOI: 10.1016/j.amjcard.2004.03.029

Genes

LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15219508-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.PMID 15219508Read ↗

Identification of novel mutations in LMNA associated with familial forms of dilated cardiomyopathy.Semantic proximity Read ↗

A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death.Semantic proximity Read ↗

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.Semantic proximity Read ↗

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.Semantic proximity Read ↗

A novel mutation of the LMNA gene in a family with dilated cardiomyopathy, conduction system disease, and sudden cardiac death of young females.Semantic proximity Read ↗

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.Semantic proximity Read ↗

Novel mutations in LMNA A/C gene and associated phenotypes.Semantic proximity Read ↗

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease.Semantic proximity Read ↗

High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.Semantic proximity Read ↗

LMNA mutations in cardiac transplant recipients.Semantic proximity Read ↗

LMNA Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated CardiomyopathySemantic proximity Read ↗

Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype.Semantic proximity Read ↗

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