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

[Relationship between congenital long QT syndrome and Brugada syndrome gene mutation].

Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae - 1 Jun 2005

Du Rong, Ren Fa-xin, Yang Jun-guo, Yuan Guo-hui, Zhang Shou-yan, Kang Cai-lian, Li Wei, Gui Le, Li Jing

Abstract excerpt

OBJECTIVE: To investigate the molecular pathology in families with long QT syndrome (LQTS) including Jervell-Longe-Nielsen syndrome (JLNS) and Romano-ward syndrome (RWS) and Brugada syndrome (BS) in Chinese population. METHODS: Polymerase chain reaction and DNA sequencing were used to screen for KCNQ1, KCNH2, KCNE1, and SCN5A mutation. RESULTS: We identified a novel mutation N1774S in the SCN5A gene of the BS...

Read the complete abstract on PubMed

Topics

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

Share to ERG1 Potassium Channel
Share to Ether-A-Go-Go Potassium Channels

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to KCNQ1 Potassium Channel

Share to Long QT Syndrome

Share to NAV1.5 Voltage-Gated Sodium Channel

Share to Potassium Channels, Voltage-Gated

Share to Romano-Ward Syndrome

Share to Sodium Channels

Source

Identifiers

PMID: 16038262

Genes

KCNQ1
KCNH2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Relationship between congenital long QT syndrome and Brugada syndrome gene mutation].PMID 16038262Read ↗

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

Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel.Semantic proximity Read ↗

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

Single nucleotide polymorphisms of the SCN5A gene in Han Chinese and their relation with Brugada syndrome.Semantic proximity Read ↗

[Sinus node dysfunction, Brugada syndrome and long QT syndrome affecting the same patient : when genetics can't make head or tail of it].Semantic proximity Read ↗

[Clinic and genetic polymorphism of Brugada syndrome in Russian patients, caused by mutation in SCN5A gene].Semantic proximity Read ↗

[Gene (SCN5A) mutation analysis of a Chinese family with Brugada syndrome].Semantic proximity Read ↗

[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome].Semantic proximity Read ↗

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

[A case of long QT syndrome with atypical clinical phenotype caused by KCNQ1-R555C missense mutation].Semantic proximity Read ↗

Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia.Semantic proximity Read ↗

Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.Semantic proximity Read ↗

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