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

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

Heart rhythm - 1 Jan 2010

Grilo Liliana Sintra, Pruvot Etienne, Grobéty Michel, Castella Vincent, Fellmann Florence, Abriel Hugues

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 Echocardiography
Share to Electrocardiography
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 Long QT Syndrome

Share to Protein Serine-Threonine Kinases

Share to Syncope

Share to Torsades de Pointes

Source

Identifiers

PMID: 20004623
DOI: 10.1016/j.hrthm.2009.09.026

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

Takotsubo cardiomyopathy and congenital long QT syndrome in a patient with a novel duplication in the Per-Arnt-Sim (PAS) domain of hERG1.PMID 20004623Read ↗

Sudden death associated with a novel H401Q PRKAG2 mutation.Semantic proximity Read ↗

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathySemantic proximity Read ↗

A common coding variant in BAG3 protects from heart failure.Semantic proximity Read ↗

Rescue of aberrant gating by a genetically encoded PAS (Per-Arnt-Sim) domain in several long QT syndrome mutant human ether-á-go-go-related gene potassium channels.Semantic proximity Read ↗

A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi–Goutiéres syndrome associated with mtDNA deletionsSemantic proximity Read ↗

PharmGKB summary: very important pharmacogene information for RYR1.Semantic proximity Read ↗

A novel hypomorphic mutation in STIM1 results in a late-onset immunodeficiency.Semantic proximity Read ↗

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

A novel kindred with inherited STAT2 deficiency and severe viral illness.Semantic proximity Read ↗

A child with branchio-oto-renal spectrum disorder carrying an SIX1 variant.Semantic proximity Read ↗

A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channelSemantic proximity Read ↗

Compound Heterozygous Truncating Variants in the BAG5 Gene As a Cause of Early-Onset Dilated Cardiomyopathy.Semantic proximity Read ↗

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