Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long‐QT syndrome | The EMBO Journal
Gene: KCNH2 (ENSG00000055118) - Summary - Homo_sapiens - Ensembl genome browser 110
IJMS | Free Full-Text | Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing | Revista Española de Cardiología
Biomolecules | Free Full-Text | Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients
Cardiac channelopathies: it's in the genes | Nature Medicine
Frontiers | Electrophysiological Characteristics of the LQT2 Syndrome Mutation KCNH2-G572S and Regulation by Accessory Protein KCNE2
A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency - ScienceDirect
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Current pharmacogenomic studies on hERG potassium channels: Trends in Molecular Medicine
Long QT Syndrome KCNH2 Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell–Derived Cardiomyocytes | Circulation: Arrhythmia and Electrophysiology
Frontiers | The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
IJMS | Free Full-Text | H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating
Functional Invalidation of Putative Sudden Infant Death Syndrome–Associated Variants in the KCNH2-Encoded Kv11.1 Channel | Circulation: Arrhythmia and Electrophysiology
Prolonged QT interval on ECG caused by hERG channel dysfunction.... | Download Scientific Diagram
Chromatogram of 453delC mutation in the KCNH2 gene (A) and schematic... | Download Scientific Diagram
KCNH2 Paralogue Annotation
Isogenic Sets of hiPSC-CMs Harboring Distinct KCNH2 Mutations Differ Functionally and in Susceptibility to Drug-Induced Arrhythmias - ScienceDirect
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome | Nature Communications
Genes | Free Full-Text | Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia
