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

[Polymorphisms of the SCN10A Gene in Patients With Sick Sinus Syndrome].

Kardiologiia - 1 Apr 2018

Niculina S Y, Marilovceva O V, Chernova A A, Tret'jakova S S, Nikulin D A, Maksimov V N

Abstract excerpt

PURPOSE: To study association of rs6795970 polymorphism of SCN10A gene with development of idiopathic sick sinus syndrome (ISSS). MATERIALS AND METHODS: We examined 109 patients with ISSS, 59 their healthy 1‑st-, 2‑nd-, and 3‑rd-degree relatives, and 630 controls. Patients with ISSS were divided into subgroups according to gender and clinical variant of the disease. All patients underwent cardiologic examination...

Read the complete abstract on PubMed

Topics

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

Share to Gene Frequency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Polymorphism, Single Nucleotide

Share to Sick Sinus Syndrome

Source

Identifiers

PMID: 29782260

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Polymorphisms of the SCN10A Gene in Patients With Sick Sinus Syndrome].PMID 29782260Read ↗

Genetic predictors of sick sinus syndrome.Semantic proximity Read ↗

[Single nucleotide polymorphism in SCN5A and the distribution in Chinese Han ethnic group].Semantic proximity Read ↗

Errata: Rare Compound Heterozygous Missense Mutation of the SCN5A Gene with Childhood-Onset Sick Sinus Syndrome in Two Chinese Sisters: A Case Report.Semantic proximity Read ↗

[Genetic predictors of sick sinus node syndrome].Semantic proximity Read ↗

[Polymorphisms of 2B-adrenergic receptor and endothelial NO-Synthase genes in genesis of the hereditary sick sinus node syndrome].Semantic proximity Read ↗

Association of human SCN5A polymorphisms with idiopathic ventricular arrhythmia in a Chinese Han cohort.Semantic proximity Read ↗

The rs6771157 C/G polymorphism in SCN10A is associated with the risk of atrial fibrillation in a Chinese Han population.Semantic proximity Read ↗

Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.Semantic proximity Read ↗

An investigation of the association of the H558R polymorphism of the SCN5A gene with idiopathic cardiac conduction disorders.Semantic proximity Read ↗

Genetic analysis of cardiac SCN5A Gene in Iranian patients with hereditary cardiac arrhythmias.Semantic proximity Read ↗

[Polymorphism of connexin 40 gene-- a novel genetic marker of the sick sinus node syndrome].Semantic proximity Read ↗

[Ser49gly polymorphism as predictor of development of hereditary sick sinus node syndrome].Semantic proximity Read ↗

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