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

Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes.

Journal of medical genetics - 1 Dec 2003

Vytopil M, Benedetti S, Ricci E, Galluzzi G, Dello Russo A, Merlini L, Boriani G, Gallina M, Morandi L, Politano L, Moggio M, Chiveri L, Hausmanova-Petrusewicz I, Ricotti R, Vohanka S, Toman J, Toniolo D

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Arrhythmias, Cardiac
Share to Cardiomyopathy, Dilated
Share to Heart Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lamin Type A

Share to Lamins

Share to Muscular Dystrophies

Share to Muscular Dystrophy, Emery-Dreifuss

Share to Nuclear Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 14684700
DOI: 10.1136/jmg.40.12.e132
PMCID: PMC1735334

Genes

LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes.PMID 14684700Read ↗

Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations.Semantic proximity Read ↗

Lamin A/C and cardiac diseases.Semantic proximity Read ↗

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

A splicing LMNA mutation causing laminopathies accompanied by aortic valve malformation.Semantic proximity Read ↗

Lamin A/C cardiomyopathy presenting as high-grade atrioventricular (AV) block, atrial fibrillation, heart failure and ventricular tachycardia in a single-family cluster.Semantic proximity Read ↗

[Diseases associated with lamin A/C gene defects: what the clinical cardiologist ought to know].Semantic proximity Read ↗

The structure and function of lamin A/C: Special focus on cardiomyopathy and therapeutic interventions.Semantic proximity Read ↗

Lamin A/C mutations in patients with dilated cardiomyopathy.Semantic proximity Read ↗

Cardiac involvement in patients with lamin A/C gene mutations: a cohort observation.Semantic proximity Read ↗

Heart involvement in lamin A/C related diseases.Semantic proximity Read ↗

Phenotypic clustering of lamin A/C mutations in neuromuscular patients.Semantic proximity Read ↗

Mutations in the LMNA gene encoding lamin A/C.Semantic proximity Read ↗

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