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

Familial Brugada Syndrome Associated With a Complete Deletion of the SCN5A and SCN10A Genes.

Revista espanola de cardiologia (English ed.) - 1 Feb 2019

Trujillo-Quintero Juan Pablo, Gutiérrez-Agulló María, Ochoa Juan Pablo, Martínez-Martínez Juan Gabriel, de Uña David, García-Fernández Amaya

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 Brugada Syndrome
Share to DNA
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Electrocardiography

Share to Genetic Predisposition to Disease

Share to NAV1.5 Voltage-Gated Sodium Channel

Share to Pedigree

Source

Identifiers

PMID: 29650450
DOI: 10.1016/j.rec.2017.12.021

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial Brugada Syndrome Associated With a Complete Deletion of the SCN5A and SCN10A Genes.PMID 29650450Read ↗

Genetics of Brugada syndrome.Semantic proximity Read ↗

The Genetics of Brugada SyndromeSemantic proximity Read ↗

[Novel SCN5A gene mutations associated with Brugada syndrome: V95I, A1649V and delF1617].Semantic proximity Read ↗

Brugada syndrome.Semantic proximity Read ↗

Identification of a novel missense SCN5A mutation in a Chinese Han family with Brugada syndrome.Semantic proximity Read ↗

New familial heterozygous c 4066_4068 delTT 2 bp deletion of the SCN5A gene causing Brugada syndrome.Semantic proximity Read ↗

Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients.Semantic proximity Read ↗

Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What’s behind the scenes?Semantic proximity Read ↗

[Genetic and molecular basis for sodium channel-mediated Brugada syndrome].Semantic proximity Read ↗

[Detection of gene mutations of SCN5A in 7 patients with Brugada syndrome].Semantic proximity Read ↗

Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?Semantic proximity Read ↗

p.D372H: A novel SCN5A mutation associated with Brugada syndromeSemantic proximity Read ↗

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