A novel KCNH2 frameshift mutation (c.46delG) associated with high risk of sudden death in a family with congenital long QT syndrome type 2 | International Journal of Arrhythmia | Full Text
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Novel mutation in the KCNH2 gene associated with long QT syndrome | Revista Portuguesa de Cardiologia (English edition)
KCNH2 Paralogue Annotation
MSTPublications: June 2020 | Medical Scientist Training Program | Vanderbilt University
Genetic analysis identified a heterozygous KCNH2 mutation. (A) Family... | Download Scientific Diagram
Frontiers | The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2
Biomolecules | Free Full-Text | Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients
Isogenic Sets of hiPSC-CMs Harboring Distinct KCNH2 Mutations Differ Functionally and in Susceptibility to Drug-Induced Arrhythmias - ScienceDirect
Modeling long QT syndrome type 2 on-a-chip via in-depth assessment of isogenic gene-edited 3D cardiac tissues | Science Advances
A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency - ScienceDirect
The novel frameshift mutation. Sequencing analysis of KCNH2 gene in the... | Download Scientific Diagram
Biomolecules | Free Full-Text | Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients
Chromatogram of 453delC mutation in the KCNH2 gene (A) and schematic... | Download Scientific Diagram
Long QT Syndrome KCNH2 Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell–Derived Cardiomyocytes | Circulation: Arrhythmia and Electrophysiology
IJMS | Free Full-Text | H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating
Overexpression KCNH2-3.1 potassium channel is associated with neuronal... | Download Scientific Diagram
Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing - Fazelifar - 2023 - Journal of Arrhythmia - Wiley Online Library
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Cellular properties of C-terminal KCNH2 long QT syndrome mutations: description and divergence from clinical phenotypes. | Semantic Scholar
Gene: KCNH2 (ENSG00000055118) - Summary - Homo_sapiens - Ensembl genome browser 110
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Generation of hiPSCs from a patient with type-2 long-QT syndrome. (A)... | Download Scientific Diagram
The KCNH2 (HERG) gene: (a)-gene chromosome location; (b)-protein... | Download Scientific Diagram
A diagram of the Kv11.1 channel trafficking pathway. KCNH2 is... | Download Scientific Diagram
