Discover Community Create You

t/gene-kcnh2

KCNH2 gene

Discuss publications and research concerning the KCNH2 gene.

0 followers0 posts29 articles

All posts discussion question review note

Create the first post

Ask a question, share an idea or link scientific evidence.

Topic rules

Follow Noodle’s community and scientific integrity rules.

Moderators

Managed by the Noodle moderation team.

Related literature

Functional characterization and allele-specific RNA interference-based rescue of KCNH2 p.F68C variant associated with long QT syndrome.
KCNH2
Effects of Spinal Versus General Anesthesia on QTc Interval and QTc Variability During Elective Cesarean Section: A Prospective Randomized Study
KCNH2
Catheter Ablation of Triggers and Arrhythmogenic Epicardial Substrates in Patients with QT Prolongation.
KCNH2
Topological Distribution of KCNH2 Variants and Genotype-Phenotype Relationship in Patients With Long QT Syndrome.
KCNH2
Deep Learning-Augmented ECG Analysis for Screening and Genotype Prediction of Congenital Long QT Syndrome.
KCNH2
Detecting QT prolongation From a Single-lead ECG With Deep Learning
KCNH2
Out-of-Hospital Cardiac Arrest Due to Ventricular Fibrillation in a 5-Year-Old Pediatric Patient.
KCNH2
Interplay Between Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome.
KCNH2
Ethnic Differences in Genetic Ion Channelopathies Associated with Sudden Cardiac Death: A Systematic Review and Meta-Analysis.
KCNH2
Considerations when using next-generation sequencing for genetic diagnosis of long-QT syndrome in the clinical testing laboratory.
KCNH2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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