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

Analysis of candidate genes for genotypic diagnosis in the long QT syndrome.

Journal of applied genetics - 1 Jan 2004

Haack Birgit, Kupka Susan, Ebauer Margret, Siemiatkowska Anna, Pfister Markus, Kwiatkowska Joanna, Ereciński Jan, Limon Janusz, Ochman Karolina, Blin Nikolaus

Abstract excerpt

Patients with the long QT syndrome (LQTS) suffer from cardiac arrhythmias that can lead to abrupt loss of consciousness and sudden death, already in young individuals. Thus, an early diagnosis of LQTS is essential for patients and their family members. So far, six genes (KCNQ1, HERG, SCN5A, ANK2, KCNE1, KCNE2) have been demonstrated to be involved in the development of LQTS. Since this syndrome is genetically...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to Chromosome Mapping

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

Share to DNA Primers

Share to KCNQ1 gene

Share to Genotype

Share to Long QT Syndrome

Share to Microsatellite Repeats

Share to Pedigree

Source

Identifiers

PMID: 15306731

Genes

ANK2
KCNQ1
SGK1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

Analysis of candidate genes for genotypic diagnosis in the long QT syndrome.PMID 15306731Read ↗

Molecular genetics of long-QT syndrome.Semantic proximity Read ↗

The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene.Semantic proximity Read ↗

Genetics of long-QT syndrome.Semantic proximity Read ↗

Cardiac ion channel gene mutations in Greek long QT syndrome patients.Semantic proximity Read ↗

Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of long QT syndrome.Semantic proximity Read ↗

[Molecular genetics of the long QT syndrome: clinical aspects].Semantic proximity Read ↗

Molecular diagnostics of families with long-QT syndrome.Semantic proximity Read ↗

Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome.Semantic proximity Read ↗

Novel KCNQ1 and HERG missense mutations in Dutch long-QT familiesSemantic proximity Read ↗

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.Semantic proximity Read ↗

Romano-Ward long QT syndrome: identification of a HERG mutation in a Taiwanese kindred.Semantic proximity Read ↗

[Value of genetic testing in the management of the congenital long QT syndrome].Semantic proximity Read ↗

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