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 | Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies
Frontiers | Electrophysiological Characteristics of the LQT2 Syndrome Mutation KCNH2-G572S and Regulation by Accessory Protein KCNE2
A diagram of the Kv11.1 channel trafficking pathway. KCNH2 is... | Download Scientific Diagram
Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long‐QT syndrome | The EMBO Journal
Frontiers | The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2
Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome | Nature Communications
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Functional Invalidation of Putative Sudden Infant Death Syndrome–Associated Variants in the KCNH2-Encoded Kv11.1 Channel | Circulation: Arrhythmia and Electrophysiology
IJMS | Free Full-Text | H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating
Modeling long QT syndrome type 2 on-a-chip via in-depth assessment of isogenic gene-edited 3D cardiac tissues | Science Advances
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency - ScienceDirect
Isogenic Sets of hiPSC-CMs Harboring Distinct KCNH2 Mutations Differ Functionally and in Susceptibility to Drug-Induced Arrhythmias - ScienceDirect
Generation of hiPSCs from a patient with type-2 long-QT syndrome. (A)... | Download Scientific Diagram
Cardiac channelopathies: it's in the genes | Nature Medicine
KCNH2 - Creative Bioarray
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing | Revista Española de Cardiología
Prolonged QT interval on ECG caused by hERG channel dysfunction.... | Download Scientific Diagram
Integrated analysis of the voltage-gated potassium channel-associated gene KCNH2 across cancers | BMC Bioinformatics | Full Text
Genetic analysis identified a heterozygous KCNH2 mutation. (A) Family... | Download Scientific Diagram
The novel frameshift mutation. Sequencing analysis of KCNH2 gene in the... | Download Scientific Diagram
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants | Circulation: Genomic and Precision Medicine
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
