Long QT Syndrome Type 1 in an Australian Indigenous Patient.

doi:10.1161/CIRCGEN.119.002813

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

Community

Back to search

Article

Long QT Syndrome Type 1 in an Australian Indigenous Patient.

Circulation. Genomic and precision medicine - 1 Apr 2020

Ganesan Anand N, Vanoye Carlos G, Alam Ferdous, Waddell-Smith Kathryn E, McGavigan Andrew D, Correnti Gemma, Haan Eric, Brown Alex, Vandenberg Jamie, George Alfred L

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 Australia
Share to KCNQ1 Potassium Channel
Share to Long QT Syndrome
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Population Groups

Share to Prognosis

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 32004091
DOI: 10.1161/CIRCGEN.119.002813
PMCID: PMC7416536

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Long QT Syndrome Type 1 in an Australian Indigenous Patient.PMID 32004091Read ↗

Clinical practice. Long-QT syndrome.Semantic proximity Read ↗

MELAS syndrome in an Indigenous Australian woman.Semantic proximity Read ↗

Short QT syndrome: from bench to bedside.Semantic proximity Read ↗

Genetic susceptibility to acquired long QT syndrome: pharmacologic challenge in first-degree relatives.Semantic proximity Read ↗

Opioid maintenance patients with QTc prolongation: congenital long QT syndrome mutation may be a contributing risk factor.Semantic proximity Read ↗

Long-QT syndrome: from genetics to management.Semantic proximity Read ↗

Long QT and Brugada syndromes: from genetics to clinical management.Semantic proximity Read ↗

Congenital Long QT syndrome.Semantic proximity Read ↗

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