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 Paralogue Annotation
The KCNH2 (HERG) gene: (a)-gene chromosome location; (b)-protein... | Download Scientific Diagram
Chromatogram of 453delC mutation in the KCNH2 gene (A) and schematic... | Download Scientific Diagram
Cardiac channelopathies: it's in the genes | Nature Medicine
Current pharmacogenomic studies on hERG potassium channels: Trends in Molecular Medicine
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Genetic analysis identified a heterozygous KCNH2 mutation. (A) Family... | 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
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Overexpression KCNH2-3.1 potassium channel is associated with neuronal... | 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
Gene: KCNH2 (ENSG00000055118) - Summary - Homo_sapiens - Ensembl genome browser 110
Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long‐QT syndrome | The EMBO Journal
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing | Revista Española de Cardiología
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Novel mutation in the KCNH2 gene associated with long QT syndrome | Revista Portuguesa de Cardiologia (English edition)
The novel frameshift mutation. Sequencing analysis of KCNH2 gene in the... | Download Scientific Diagram
Generation of hiPSCs from a patient with type-2 long-QT syndrome. (A)... | Download Scientific Diagram
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
A diagram of the Kv11.1 channel trafficking pathway. KCNH2 is... | 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
Prolonged QT interval on ECG caused by hERG channel dysfunction.... | Download Scientific Diagram
Modeling long QT syndrome type 2 on-a-chip via in-depth assessment of isogenic gene-edited 3D cardiac tissues | Science Advances
