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
Frontiers | Electrophysiological Characteristics of the LQT2 Syndrome Mutation KCNH2-G572S and Regulation by Accessory Protein KCNE2
Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology | bioRxiv
Integrated analysis of the voltage-gated potassium channel-associated gene KCNH2 across cancers | BMC Bioinformatics | Full Text
Long QT Syndrome KCNH2 Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell–Derived Cardiomyocytes | Circulation: Arrhythmia and Electrophysiology
Tbx20 controls the expression of the KCNH2 gene and of hERG channels | PNAS
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
The novel frameshift mutation. Sequencing analysis of KCNH2 gene in the... | Download Scientific Diagram
A diagram of the Kv11.1 channel trafficking pathway. KCNH2 is... | Download Scientific Diagram
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
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
Genetic analysis identified a heterozygous KCNH2 mutation. (A) Family... | Download Scientific Diagram
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Novel mutation in the KCNH2 gene associated with long QT syndrome | Revista Portuguesa de Cardiologia (English edition)
Biomolecules | Free Full-Text | Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients
KCNH2-HERG channel subunit. Localization of the described mutations. | Download Scientific Diagram
Overexpression KCNH2-3.1 potassium channel is associated with neuronal... | Download Scientific Diagram
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing | Revista Española de Cardiología
Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long‐QT syndrome | The EMBO Journal
Biomolecules | Free Full-Text | Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients
Frontiers | The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2
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
