TY  - JOUR
AU  - Moreno-Manuel, Ana I
AU  - Macias, Alvaro
AU  - Cruz, Francisco Miguel
AU  - Gutiérrez, Lilian K
AU  - Martínez, Fernando
AU  - González-Guerra, Andrés
AU  - Martinez-Carrascoso, Isabel
AU  - Bermúdez-Jimenez, Francisco José
AU  - Sánchez-Pérez, Patricia
AU  - Vera-Pedrosa, María Linarejos
AU  - Ruiz, Juan Manuel
AU  - Bernal, Juan Antonio
AU  - Jalife, Jose
PY  - 2024
DO  - 10.1093/cvr/cvae019
UR  - http://hdl.handle.net/20.500.12105/19244
AB  - AIMSShort QT Syndrome Type 3 (SQTS3) is a rare arrhythmogenic disease caused by gain-of-function mutations in KCNJ2, the gene coding the inward rectifier potassium channel Kir2.1. We used a multidisciplinary approach and investigated arrhythmogenic...
LA  - eng
PB  - Oxford University Press
TI  - The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of Short QT Syndrome type 3.
TY  - journal article
ER  -