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

Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation.

Anatolian journal of cardiology - 1 Jul 2018

Adadi Najlae, Radi Fatima Zohra, Lahrouchi Najim, Hara Loubna, Ratbi Ilham, Elalaoui Siham Chafai, Alders Marielle, Zarzur Jamila, Bezzina Connie, Sefiani Abdelaziz

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 Adolescent
Share to Cardiomyopathy, Dilated
Share to Child
Share to Echocardiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lamin Type A

Share to Morocco

Share to Pedigree

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 29952368
DOI: 10.14744/AnatolJCardiol.2018.69639
PMCID: PMC6237802

Genes

LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation.PMID 29952368Read ↗

Cardiomyopathy with LMNA Mutation.Semantic proximity Read ↗

Thirty-five-year follow-up of 3 generations of a family with LMNA cardiomyopathy.Semantic proximity Read ↗

LMNA Mutation in a Family with a Strong History of Sudden Cardiac Death.Semantic proximity Read ↗

A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family.Semantic proximity Read ↗

Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.Semantic proximity Read ↗

LMNA Q353R Mutation Causes Dilated Cardiomyopathy Through Impaired Vitamin D Signaling.Semantic proximity Read ↗

The novel pathogenic variant in the LMNA gene in a four-generation family with sudden deaths and cardiomyopathy: Utility of molecular autopsy.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 ↗

LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies.Semantic proximity Read ↗

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

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

Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies.Semantic proximity Read ↗

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