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

A Rare Cause of Syncope: Naxos Disease Caused by Novel Homozygous Deletion in the JUP Gene.

Circulation. Cardiovascular imaging - 1 Oct 2021

Sonsöz Mehmet Rasih, İli Ezgi Gökpinar, Gezdirici Alper, Topel Cagdas, Kahveci Gökhan, Bornaun Helen

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 Arrhythmogenic Right Ventricular Dysplasia
Share to gamma Catenin
Share to Hair Diseases
Share to Heart Ventricles

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Keratoderma, Palmoplantar

Share to Magnetic Resonance Imaging, Cine

Share to Rare Diseases

Share to Syncope

Source

Identifiers

PMID: 34587761
DOI: 10.1161/CIRCIMAGING.121.013059

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Rare Cause of Syncope: Naxos Disease Caused by Novel Homozygous Deletion in the JUP Gene.PMID 34587761Read ↗

Cardiomyopathy diagnosed in the eldest child harbouring p.S24X mutation in JUP.Semantic proximity Read ↗

Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.Semantic proximity Read ↗

Syncope update 2013: diagnosis and treatment.Semantic proximity Read ↗

Genetic mutations in young patients admitted to an emergency department for syncope during sport practice.Semantic proximity Read ↗

Unique post-exercise electrophysiological test results in a new Andersen-Tawil syndrome mutation.Semantic proximity Read ↗

Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.Semantic proximity Read ↗

Know thy neighbor: a survey of diseases and complex syndromes that map to chromosomal regions encoding TRP channels.Semantic proximity Read ↗

Genetic variants associated with syncope implicate neural and autonomic processesSemantic proximity Read ↗

Takotsubo cardiomyopathy and congenital long QT syndrome in a patient with a novel duplication in the Per-Arnt-Sim (PAS) domain of hERG1.Semantic proximity Read ↗

Gain-of-function mutations in STIM1 and ORAI1 causing tubular aggregate myopathy and Stormorken syndromeSemantic proximity Read ↗

Chronic pain in Noonan Syndrome: A previously unreported but common symptom.Semantic proximity Read ↗

An RyR2 mutation found in a family with a short-coupled variant of torsade de pointes.Semantic proximity Read ↗

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